{
  "id": 19320,
  "label": "autosomal recessive non-syndromic intellectual disability",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019502",
  "properties": {
    "xrefs": [
      "DOID:0060308",
      "GARD:0018643",
      "MEDGEN:1826073",
      "OMIMPS:249500",
      "Orphanet:88616",
      "UMLS:C5680181"
    ],
    "synonyms": [
      "autosomal recessive intellectual disability",
      "intellectual disability, autosomal recessive",
      "AR-NSID",
      "NS-ARID",
      "autosomal recessive non-syndromic intellectual disability",
      "mental retardation, autosomal recessive",
      "non-syndromic intellectual disability, autosomal recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Autosomal recessive form of non-syndromic intellectual disability."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 68,
  "parents": [
    {
      "id": 2962,
      "label": "non-syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050889"
        ],
        "synonyms": [
          "isolated intellectual disability",
          "nonsyndromic intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An intellectual disability that is not part of a larger syndrome."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000509"
    },
    {
      "id": 17944,
      "label": "disorder of carbohydrate transmembrane transport and absorption",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19082
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021313",
          "MEDGEN:1842168",
          "Orphanet:309001",
          "UMLS:C5681069",
          "icd11.foundation:1315315105"
        ],
        "synonyms": [
          "disorder of carbohydrate absorption and transport"
        ]
      },
      "child_count": 14,
      "reference_id": "MONDO:0017706"
    },
    {
      "id": 24319,
      "label": "intellectual disability, autosomal recessive",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3324,
        7611,
        24226
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A broad category of disorders characterized by an impairment to the intelligence an individual possesses, caused by an autosomal recessive genetic disorder."
      },
      "child_count": 9,
      "reference_id": "MONDO:0100597"
    }
  ],
  "children": [
    {
      "id": 10801,
      "label": "intellectual disability, autosomal recessive 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081177",
          "GARD:0022537",
          "MEDGEN:344468",
          "MESH:C565406",
          "OMIM:249500",
          "UMLS:C1855304"
        ],
        "synonyms": [
          "PRSS12 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in PRSS12",
          "intellectual disability, autosomal recessive 1",
          "intellectual disability, autosomal recessive type 1",
          "mental retardation, autosomal recessive type 1",
          "MRT1",
          "mental retardation, autosomal recessive 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PRSS12 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009580"
    },
    {
      "id": 12909,
      "label": "intellectual disability, autosomal recessive 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081178",
          "GARD:0022538",
          "MEDGEN:334541",
          "MESH:C564404",
          "OMIM:607417",
          "UMLS:C1843942"
        ],
        "synonyms": [
          "CRBN autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN",
          "intellectual disability, autosomal recessive 2",
          "intellectual disability, autosomal recessive type 2",
          "mental retardation, autosomal recessive type 2",
          "MRT2",
          "intellectual disability, autosomal recessive 2A",
          "mental retardation, autosomal recessive 2",
          "mental retardation, autosomal recessive 2A"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRBN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011828"
    },
    {
      "id": 13105,
      "label": "intellectual disability, autosomal recessive 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081179",
          "GARD:0022539",
          "MEDGEN:373870",
          "MESH:C563929",
          "OMIM:608443",
          "UMLS:C1838023"
        ],
        "synonyms": [
          "CC2D1A autosomal recessive non-syndromic intellectual disability",
          "MRT3",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A",
          "intellectual disability, autosomal recessive 3",
          "intellectual disability, autosomal recessive type 3",
          "mental retardation, autosomal recessive 3",
          "mental retardation, autosomal recessive type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CC2D1A gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012037"
    },
    {
      "id": 13659,
      "label": "intellectual disability, autosomal recessive 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4427,
        19320,
        26279
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081180",
          "GARD:0022540",
          "MEDGEN:370850",
          "MESH:C567019",
          "OMIM:611090",
          "UMLS:C1970200"
        ],
        "synonyms": [
          "intellectual developmental disorder, autosomal recessive 12",
          "intellectual disability, autosomal recessive 12",
          "intellectual disability, autosomal recessive type 12",
          "mental retardation, autosomal recessive type 12",
          "MRT12",
          "mental retardation, autosomal recessive 12"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012612"
    },
    {
      "id": 13660,
      "label": "intellectual disability, autosomal recessive 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081181",
          "GARD:0022541",
          "MEDGEN:370849",
          "MESH:C567018",
          "OMIM:611091",
          "UMLS:C1970199"
        ],
        "synonyms": [
          "NSUN2 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2",
          "intellectual disability, autosomal recessive 5",
          "intellectual disability, autosomal recessive type 5",
          "mental retardation, autosomal recessive type 5",
          "MRT5",
          "mental retardation, autosomal recessive 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NSUN2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012613"
    },
    {
      "id": 13661,
      "label": "intellectual disability, autosomal recessive 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081182",
          "GARD:0022542",
          "MEDGEN:370848",
          "MESH:C567017",
          "OMIM:611092",
          "UMLS:C1970198"
        ],
        "synonyms": [
          "GRIK2 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in GRIK2",
          "intellectual developmental disorder, autosomal recessive 6",
          "intellectual disability, autosomal recessive 6",
          "intellectual disability, autosomal recessive type 6",
          "mental retardation, autosomal recessive type 6",
          "MRT6",
          "mental retardation, autosomal recessive 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIK2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012614"
    },
    {
      "id": 13662,
      "label": "intellectual disability, autosomal recessive 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081183",
          "GARD:0022543",
          "MEDGEN:370847",
          "MESH:C567016",
          "OMIM:611093",
          "UMLS:C1970197"
        ],
        "synonyms": [
          "TUSC3 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in TUSC3",
          "intellectual disability, autosomal recessive 7",
          "intellectual disability, autosomal recessive type 7",
          "mental retardation, autosomal recessive type 7",
          "MRT7",
          "intellectual disability, autosomal recessive 22",
          "mental retardation, autosomal recessive 22",
          "mental retardation, autosomal recessive 7"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TUSC3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012615"
    },
    {
      "id": 13663,
      "label": "intellectual disability, autosomal recessive 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081184",
          "GARD:0022544",
          "MEDGEN:369678",
          "MESH:C567014",
          "OMIM:611095",
          "UMLS:C1970195"
        ],
        "synonyms": [
          "MRT9",
          "intellectual disability, autosomal recessive 9",
          "mental retardation, autosomal recessive, 9/26",
          "intellectual disability, autosomal recessive 26",
          "mental retardation, autosomal recessive 26",
          "mental retardation, autosomal recessive 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012617"
    },
    {
      "id": 13664,
      "label": "intellectual disability, autosomal recessive 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081185",
          "GARD:0022545",
          "MEDGEN:410010",
          "MESH:C567013",
          "OMIM:611096",
          "UMLS:C1970194"
        ],
        "synonyms": [
          "MRT10",
          "intellectual disability, autosomal recessive 10",
          "mental retardation, autosomal recessive 10/20",
          "intellectual disability, autosomal recessive 20",
          "mental retardation, autosomal recessive 10",
          "mental retardation, autosomal recessive 20"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012618"
    },
    {
      "id": 13665,
      "label": "intellectual disability, autosomal recessive 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081186",
          "GARD:0022546",
          "MEDGEN:369677",
          "MESH:C567012",
          "OMIM:611097",
          "UMLS:C1970193"
        ],
        "synonyms": [
          "MRT11",
          "intellectual disability, autosomal recessive 11",
          "mental retardation, autosomal recessive, 11",
          "mental retardation, autosomal recessive 11"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012619"
    },
    {
      "id": 13669,
      "label": "intellectual disability, autosomal recessive 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081187",
          "GARD:0022547",
          "MEDGEN:370844",
          "MESH:C567008",
          "OMIM:611107",
          "UMLS:C1970179"
        ],
        "synonyms": [
          "MRT4",
          "intellectual disability, autosomal recessive 4",
          "mental retardation, autosomal recessive, 4",
          "mental retardation, autosomal recessive 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012623"
    },
    {
      "id": 14209,
      "label": "intellectual disability, autosomal recessive 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081098",
          "GARD:0022548",
          "MEDGEN:442564",
          "MESH:C567714",
          "OMIM:613192",
          "UMLS:C2750791"
        ],
        "synonyms": [
          "TRAPPC9 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9",
          "intellectual disability, autosomal recessive 13",
          "intellectual disability, autosomal recessive type 13",
          "mental retardation, autosomal recessive type 13",
          "MRT13",
          "mental retardation, autosomal recessive 13"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TRAPPC9 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013173"
    },
    {
      "id": 14557,
      "label": "intellectual disability, autosomal recessive 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081188",
          "GARD:0022549",
          "MEDGEN:462812",
          "OMIM:614020",
          "UMLS:C3151462"
        ],
        "synonyms": [
          "TECR autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in TECR",
          "intellectual disability, autosomal recessive 14",
          "intellectual disability, autosomal recessive type 14",
          "mental retardation, autosomal recessive type 14",
          "MRT14",
          "mental retardation, autosomal recessive 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TECR gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013528"
    },
    {
      "id": 14649,
      "label": "Rafiq syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081097",
          "GARD:0022550",
          "MEDGEN:481757",
          "OMIM:614202",
          "UMLS:C3280127"
        ],
        "synonyms": [
          "CDG2U",
          "MAN1B1 autosomal recessive non-syndromic intellectual disability",
          "RAFQS",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in MAN1B1",
          "intellectual disability, autosomal recessive 15",
          "mental retardation, autosomal recessive 15",
          "mental retardation, autosomal recessive type 15",
          "MRT15"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MAN1B1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013624"
    },
    {
      "id": 14654,
      "label": "intellectual disability, autosomal recessive 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081189",
          "GARD:0022551",
          "MEDGEN:481784",
          "OMIM:614208",
          "UMLS:C3280154"
        ],
        "synonyms": [
          "MRT16",
          "intellectual disability, autosomal recessive 16",
          "mental retardation, autosomal recessive 16"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013629"
    },
    {
      "id": 14675,
      "label": "intellectual disability, autosomal recessive 18",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081190",
          "GARD:0022552",
          "MEDGEN:481895",
          "OMIM:614249",
          "UMLS:C3280265"
        ],
        "synonyms": [
          "MED23 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in MED23",
          "intellectual developmental disorder, autosomal recessive 18, with or without epilepsy",
          "intellectual disability, autosomal recessive 18",
          "intellectual disability, autosomal recessive type 18",
          "mental retardation, autosomal recessive type 18",
          "MED23",
          "MRT18",
          "autosomal recessive nonsyndromic intellectual disability-18",
          "autosomal recessive nonsyndromic mental retardation-18",
          "mental retardation, autosomal recessive 18"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MED23 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013651"
    },
    {
      "id": 14716,
      "label": "intellectual disability, autosomal recessive 31",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081191",
          "GARD:0022553",
          "MEDGEN:482153",
          "OMIM:614329",
          "UMLS:C3280523"
        ],
        "synonyms": [
          "MRT31",
          "intellectual disability, autosomal recessive 31",
          "mental retardation, autosomal recessive 31"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013694"
    },
    {
      "id": 14719,
      "label": "intellectual disability, autosomal recessive 29",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081192",
          "GARD:0022554",
          "MEDGEN:482155",
          "OMIM:614333",
          "UMLS:C3280525"
        ],
        "synonyms": [
          "MRT29",
          "intellectual disability, autosomal recessive 29",
          "mental retardation, autosomal recessive 29"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013697"
    },
    {
      "id": 14723,
      "label": "intellectual disability, autosomal recessive 27",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081193",
          "GARD:0022555",
          "MEDGEN:482168",
          "OMIM:614340",
          "UMLS:C3280538"
        ],
        "synonyms": [
          "LINS1 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in LINS1",
          "intellectual developmental disorder, autosomal recessive 27",
          "intellectual disability, autosomal recessive 27",
          "intellectual disability, autosomal recessive type 27",
          "mental retardation, autosomal recessive type 27",
          "MRT27",
          "mental retardation, autosomal recessive 27"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LINS1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013702"
    },
    {
      "id": 14724,
      "label": "intellectual disability, autosomal recessive 33",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081194",
          "GARD:0022556",
          "MEDGEN:482169",
          "OMIM:614341",
          "UMLS:C3280539"
        ],
        "synonyms": [
          "MRT33",
          "intellectual disability, autosomal recessive 33",
          "mental retardation, autosomal recessive 33"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013703"
    },
    {
      "id": 14725,
      "label": "intellectual disability, autosomal recessive 30",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081195",
          "GARD:0022557",
          "MEDGEN:482170",
          "OMIM:614342",
          "UMLS:C3280540"
        ],
        "synonyms": [
          "MRT30",
          "intellectual disability, autosomal recessive 30",
          "mental retardation, autosomal recessive 30"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013704"
    },
    {
      "id": 14726,
      "label": "intellectual disability, autosomal recessive 19",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022558",
          "MEDGEN:482171",
          "OMIM:614343",
          "UMLS:C3280541"
        ],
        "synonyms": [
          "MRT19",
          "intellectual disability, autosomal recessive 19",
          "mental retardation, autosomal recessive 19"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013705"
    },
    {
      "id": 14727,
      "label": "intellectual disability, autosomal recessive 23",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081196",
          "GARD:0022559",
          "MEDGEN:482172",
          "OMIM:614344",
          "UMLS:C3280542"
        ],
        "synonyms": [
          "MRT23",
          "intellectual disability, autosomal recessive 23",
          "mental retardation, autosomal recessive 23"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013706"
    },
    {
      "id": 14728,
      "label": "intellectual disability, autosomal recessive 24",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081197",
          "GARD:0022560",
          "MEDGEN:482173",
          "OMIM:614345",
          "UMLS:C3280543"
        ],
        "synonyms": [
          "MRT24",
          "intellectual disability, autosomal recessive 24",
          "mental retardation, autosomal recessive 24"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013707"
    },
    {
      "id": 14729,
      "label": "intellectual disability, autosomal recessive 25",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081198",
          "GARD:0022561",
          "MEDGEN:482174",
          "OMIM:614346",
          "UMLS:C3280544"
        ],
        "synonyms": [
          "MRT25",
          "intellectual disability, autosomal recessive 25",
          "mental retardation, autosomal recessive 25"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013708"
    },
    {
      "id": 14730,
      "label": "intellectual disability, autosomal recessive 28",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081199",
          "GARD:0022562",
          "MEDGEN:482175",
          "OMIM:614347",
          "UMLS:C3280545"
        ],
        "synonyms": [
          "MRT28",
          "intellectual disability, autosomal recessive 28",
          "mental retardation, autosomal recessive 28"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013709"
    },
    {
      "id": 14803,
      "label": "intellectual disability, autosomal recessive 34",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081200",
          "GARD:0022563",
          "MEDGEN:482674",
          "NCIT:C153179",
          "OMIM:614499",
          "UMLS:C3281044"
        ],
        "synonyms": [
          "CRADD autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD",
          "intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly",
          "intellectual disability, autosomal recessive 34",
          "intellectual disability, autosomal recessive type 34",
          "mental retardation, autosomal recessive type 34",
          "MRT34",
          "intellectual disability, autosomal recessive 34, with variant lissencephaly",
          "mental retardation, autosomal recessive 34",
          "mental retardation, autosomal recessive 34, with variant lissencephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRADD gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013785"
    },
    {
      "id": 15350,
      "label": "intellectual disability, autosomal recessive 42",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022564",
          "MEDGEN:862780",
          "OMIM:615802",
          "UMLS:C4014343"
        ],
        "synonyms": [
          "PGAP1 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1",
          "intellectual disability, autosomal recessive 42",
          "intellectual disability, autosomal recessive type 42",
          "mental retardation, autosomal recessive type 42",
          "neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities",
          "MRT42",
          "glycosylphosphatidylinositol biosynthesis defect 9",
          "mental retardation, autosomal recessive 42"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PGAP1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014348"
    },
    {
      "id": 15356,
      "label": "intellectual disability, autosomal recessive 43",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081207",
          "GARD:0022565",
          "MEDGEN:862823",
          "OMIM:615817",
          "UMLS:C4014386"
        ],
        "synonyms": [
          "WASHC4 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in WASHC4",
          "intellectual developmental disorder, autosomal recessive 43",
          "intellectual disability, autosomal recessive 43",
          "intellectual disability, autosomal recessive type 43",
          "mental retardation, autosomal recessive type 43",
          "MRT43",
          "mental retardation, autosomal recessive 43"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the WASHC4 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014354"
    },
    {
      "id": 15411,
      "label": "intellectual disability, autosomal recessive 44",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081208",
          "GARD:0022566",
          "MEDGEN:863182",
          "OMIM:615942",
          "UMLS:C4014745"
        ],
        "synonyms": [
          "METTL23 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in METTL23",
          "intellectual disability, autosomal recessive 44",
          "intellectual disability, autosomal recessive type 44",
          "mental retardation, autosomal recessive type 44",
          "MRT44",
          "mental retardation, autosomal recessive 44"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the METTL23 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014409"
    },
    {
      "id": 15430,
      "label": "intellectual disability, autosomal recessive 45",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081209",
          "GARD:0022567",
          "MEDGEN:863301",
          "OMIM:615979",
          "UMLS:C4014864"
        ],
        "synonyms": [
          "FBXO31 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in FBXO31",
          "intellectual disability, autosomal recessive 45",
          "intellectual disability, autosomal recessive type 45",
          "mental retardation, autosomal recessive type 45",
          "MRT45",
          "mental retardation, autosomal recessive 45"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FBXO31 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014430"
    },
    {
      "id": 15498,
      "label": "intellectual disability, autosomal recessive 46",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081210",
          "GARD:0022568",
          "MEDGEN:863720",
          "OMIM:616116",
          "UMLS:C4015283"
        ],
        "synonyms": [
          "NDST1 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in NDST1",
          "intellectual disability, autosomal recessive 46",
          "intellectual disability, autosomal recessive type 46",
          "mental retardation, autosomal recessive type 46",
          "MRT46",
          "mental retardation, autosomal recessive 46"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NDST1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014499"
    },
    {
      "id": 15523,
      "label": "intellectual disability, autosomal recessive 47",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081211",
          "GARD:0022569",
          "MEDGEN:863881",
          "OMIM:616193",
          "UMLS:C4015444"
        ],
        "synonyms": [
          "FMN2 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2",
          "intellectual developmental disorder, autosomal recessive 47",
          "intellectual disability, autosomal recessive 47",
          "intellectual disability, autosomal recessive type 47",
          "mental retardation, autosomal recessive type 47",
          "MRT47",
          "mental retardation, autosomal recessive 47"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FMN2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014524"
    },
    {
      "id": 15644,
      "label": "Al-Raqad syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025009",
          "MEDGEN:897610",
          "OMIM:616459",
          "UMLS:C4085595"
        ],
        "synonyms": [
          "Al-Raqad syndrome",
          "AL-RAQAD syndrome",
          "ARS"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014648"
    },
    {
      "id": 15645,
      "label": "intellectual disability, autosomal recessive 50",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081213",
          "GARD:0022570",
          "MEDGEN:906893",
          "OMIM:616460",
          "UMLS:C4225319"
        ],
        "synonyms": [
          "EDC3 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in EDC3",
          "intellectual developmental disorder, autosomal recessive 50",
          "intellectual disability, autosomal recessive 50",
          "intellectual disability, autosomal recessive type 50",
          "mental retardation, autosomal recessive type 50",
          "MRT50",
          "mental retardation, autosomal recessive 50"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the EDC3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014649"
    },
    {
      "id": 15750,
      "label": "intellectual disability, autosomal recessive 51",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081214",
          "GARD:0022571",
          "MEDGEN:903243",
          "OMIM:616739",
          "UMLS:C4225220"
        ],
        "synonyms": [
          "HNMT autosomal recessive non-syndromic intellectual disability",
          "MRT51",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT",
          "intellectual developmental disorder, autosomal recessive 51",
          "intellectual disability, autosomal recessive 51",
          "intellectual disability, autosomal recessive type 51",
          "mental retardation, autosomal recessive 51",
          "mental retardation, autosomal recessive type 51"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the HNMT gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014759"
    },
    {
      "id": 15802,
      "label": "intellectual disability, autosomal recessive 52",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081215",
          "GARD:0022572",
          "MEDGEN:903181",
          "OMIM:616887",
          "UMLS:C4225168"
        ],
        "synonyms": [
          "LMAN2L autosomal recessive non-syndromic intellectual disability",
          "MRT52",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L",
          "intellectual developmental disorder, autosomal recessive 52",
          "intellectual disability, autosomal recessive 52",
          "intellectual disability, autosomal recessive type 52",
          "mental retardation, autosomal recessive 52",
          "mental retardation, autosomal recessive type 52"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LMAN2L gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014815"
    },
    {
      "id": 15858,
      "label": "intellectual disability, autosomal recessive 54",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081216",
          "GARD:0022573",
          "MEDGEN:934722",
          "OMIM:617028",
          "UMLS:C4310755"
        ],
        "synonyms": [
          "MRT54",
          "TNIK autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in TNIK",
          "intellectual developmental disorder 54",
          "intellectual disability, autosomal recessive 54",
          "intellectual disability, autosomal recessive type 54",
          "mental retardation, autosomal recessive 54",
          "mental retardation, autosomal recessive type 54"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TNIK gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014876"
    },
    {
      "id": 15909,
      "label": "intellectual disability, autosomal recessive 56",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081217",
          "GARD:0022574",
          "MEDGEN:934670",
          "OMIM:617125",
          "UMLS:C4310703"
        ],
        "synonyms": [
          "MRT56",
          "ZC3H14 autosomal recessive non-syndromic intellectual disability",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in ZC3H14",
          "intellectual developmental disorder, autosomal recessive 56",
          "intellectual disability, autosomal recessive 56",
          "intellectual disability, autosomal recessive type 56",
          "mental retardation, autosomal recessive 56",
          "mental retardation, autosomal recessive type 56"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the ZC3H14 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014930"
    },
    {
      "id": 15930,
      "label": "intellectual developmental disorder, autosomal recessive 74",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081218",
          "DOID:0112104",
          "GARD:0016208",
          "MEDGEN:934651",
          "OMIM:617169",
          "UMLS:C4310684"
        ],
        "synonyms": [
          "APC2 Sotos syndrome",
          "Sotos syndrome caused by mutation in APC2",
          "Sotos syndrome type 3",
          "intellectual developmental disorder, autosomal recessive 74"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the APC2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014951"
    },
    {
      "id": 15941,
      "label": "intellectual disability, autosomal recessive 57",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081219",
          "GARD:0022575",
          "MEDGEN:934640",
          "OMIM:617188",
          "UMLS:C4310673"
        ],
        "synonyms": [
          "MBOAT7 autosomal recessive non-syndromic intellectual disability",
          "MRT57",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in MBOAT7",
          "intellectual developmental disorder, autosomal recessive 57",
          "intellectual disability, autosomal recessive 57",
          "intellectual disability, autosomal recessive type 57",
          "mental retardation, autosomal recessive 57",
          "mental retardation, autosomal recessive type 57"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MBOAT7 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014962"
    },
    {
      "id": 15972,
      "label": "intellectual disability, autosomal recessive 58",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081220",
          "GARD:0013361",
          "MEDGEN:934608",
          "OMIM:617270",
          "UMLS:C4310641"
        ],
        "synonyms": [
          "ELP2 autosomal recessive non-syndromic intellectual disability",
          "MRT58",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2",
          "intellectual developmental disorder, autosomal recessive 58",
          "intellectual disability, autosomal recessive 58",
          "intellectual disability, autosomal recessive type 58",
          "mental retardation, autosomal recessive 58",
          "mental retardation, autosomal recessive type 58",
          "ELP2-related disorder",
          "autosomal recessive intellectual disability 58"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the ELP2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014996"
    },
    {
      "id": 15996,
      "label": "intellectual disability, autosomal recessive 59",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081221",
          "GARD:0025053",
          "MEDGEN:934586",
          "OMIM:617323",
          "UMLS:C4310619"
        ],
        "synonyms": [
          "IMPA1 autosomal recessive non-syndromic intellectual disability",
          "MRT59",
          "autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1",
          "intellectual disability, autosomal recessive 59",
          "intellectual disability, autosomal recessive type 59",
          "mental retardation, autosomal recessive 59",
          "mental retardation, autosomal recessive type 59"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the IMPA1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015020"
    },
    {
      "id": 16924,
      "label": "pontocerebellar hypoplasia type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16198,
        16736,
        19320,
        19752
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112322",
          "GARD:0010704",
          "MEDGEN:1780208",
          "MESH:C548069",
          "Orphanet:2254",
          "SCTID:718610008",
          "UMLS:C5442006",
          "icd11.foundation:1227773923"
        ],
        "synonyms": [
          "MRT32",
          "Norman disease",
          "PCH1",
          "mental retardation, autosomal recessive 32"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Pontocerebellar hypoplasia type 1 (PCH1), also known as Norman's disease, is a clinically and genetically heterogeneous group of autosomal recessive disorders with a prenatal onset characterized by diffuse muscular atrophy secondary to pontocerebellar hypoplasia and spinal cord anterior horn cell degeneration resulting in early death."
      },
      "child_count": 12,
      "reference_id": "MONDO:0016396"
    },
    {
      "id": 20227,
      "label": "intellectual disability, autosomal recessive 64",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081225",
          "GARD:0025261",
          "MEDGEN:1648279",
          "OMIM:618103",
          "UMLS:C4748192"
        ],
        "synonyms": [
          "MENTAL RETARDATION, autosomal recessive 64",
          "MRT64"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020846"
    },
    {
      "id": 20231,
      "label": "intellectual disability, autosomal recessive 65",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081226",
          "GARD:0022578",
          "MEDGEN:1648401",
          "OMIM:618109",
          "UMLS:C4748219"
        ],
        "synonyms": [
          "MRT65",
          "intellectual disability, autosomal recessive 65",
          "mental retardation, autosomal recessive 65"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020850"
    },
    {
      "id": 21972,
      "label": "intellectual developmental disorder, autosomal recessive 73",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081233",
          "GARD:0025596",
          "MEDGEN:1802013",
          "OMIM:619717",
          "UMLS:C5676902"
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        "synonyms": [
          "MRT73"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030533"
    },
    {
      "id": 22043,
      "label": "intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081234",
          "GARD:0025637",
          "MEDGEN:1808159",
          "OMIM:619827",
          "UMLS:C5676961"
        ],
        "synonyms": [
          "MRT75",
          "intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030785"
    },
    {
      "id": 22120,
      "label": "intellectual disability, autosomal recessive 61",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080239",
          "GARD:0025660",
          "MEDGEN:1622296",
          "OMIM:617773",
          "UMLS:C4540424"
        ],
        "synonyms": [
          "intellectual disability, autosomal recessive 61",
          "Alwadei syndrome",
          "MRT61",
          "autosomal recessive intellectual disability 61",
          "autosomal recessive mental retardation 61",
          "mental retardation, autosomal recessive 61"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13."
      },
      "child_count": 0,
      "reference_id": "MONDO:0030915"
    },
    {
      "id": 22155,
      "label": "intellectual developmental disorder, autosomal recessive 76",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081235",
          "GARD:0025669",
          "MEDGEN:1808571",
          "OMIM:619931",
          "UMLS:C5677007"
        ],
        "synonyms": [
          "MRT76",
          "intellectual developmental disorder, autosomal recessive 76",
          "mental retardation, autosomal recessive 76"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030968"
    },
    {
      "id": 22203,
      "label": "intellectual developmental disorder, autosomal recessive 77",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081236",
          "GARD:0025679",
          "MEDGEN:1823966",
          "OMIM:619988",
          "UMLS:C5774193"
        ],
        "synonyms": [
          "MRT77",
          "intellectual developmental disorder, autosomal recessive 77"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0031031"
    },
    {
      "id": 22289,
      "label": "intellectual disability, autosomal recessive 66",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081227",
          "GARD:0022579",
          "MEDGEN:1648460",
          "OMIM:618221",
          "UMLS:C4748732"
        ],
        "synonyms": [
          "intellectual developmental disorder, autosomal recessive 66",
          "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66",
          "MRT66"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032605"
    },
    {
      "id": 22342,
      "label": "intellectual developmental disorder, autosomal recessive 67",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081228",
          "GARD:0025716",
          "MEDGEN:1648350",
          "OMIM:618295",
          "UMLS:C4749019"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67",
          "MRT67",
          "Mental Retardation, Autosomal Recessive 67"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032662"
    },
    {
      "id": 22345,
      "label": "intellectual developmental disorder, autosomal recessive 68",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081229",
          "GARD:0025718",
          "MEDGEN:1648490",
          "OMIM:618302",
          "UMLS:C4749033"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68",
          "MRT68",
          "Mental Retardation, Autosomal Recessive 68"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032665"
    },
    {
      "id": 22382,
      "label": "intellectual developmental disorder, autosomal recessive 69",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081230",
          "GARD:0025727",
          "MEDGEN:1676539",
          "OMIM:618383",
          "Orphanet:699835",
          "UMLS:C5193067"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 69",
          "MRT69",
          "Mental Retardation, Autosomal Recessive 69"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032715"
    },
    {
      "id": 22391,
      "label": "intellectual developmental disorder, autosomal recessive 70",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081231",
          "GARD:0022580",
          "MEDGEN:1679317",
          "OMIM:618402",
          "UMLS:C5193077"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 70",
          "MRT70",
          "Mental Retardation, Autosomal Recessive 70"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032729"
    },
    {
      "id": 22446,
      "label": "intellectual developmental disorder, autosomal recessive 71",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081232",
          "GARD:0025744",
          "MEDGEN:1673448",
          "OMIM:618504",
          "UMLS:C5193133"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 71",
          "MRT71",
          "Mental Retardation, Autosomal Recessive 71"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032789"
    },
    {
      "id": 22513,
      "label": "intellectual developmental disorder, autosomal recessive 72",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080765",
          "GARD:0025761",
          "MEDGEN:1684805",
          "OMIM:618665",
          "UMLS:C5231452"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72",
          "MRT72",
          "Mental Retardation, Autosomal Recessive 72"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032860"
    },
    {
      "id": 22992,
      "label": "glycosylphosphatidylinositol biosynthesis defect 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4594,
        19320,
        21353
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081223",
          "GARD:0022577",
          "MEDGEN:1628197",
          "OMIM:617816",
          "UMLS:C4540521"
        ],
        "synonyms": [
          "glycosylphosphatidylinositol biosynthesis defect 16",
          "GPIBD16",
          "intellectual disability, autosomal recessive 62",
          "mental retardation, autosomal recessive 62"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0040500"
    },
    {
      "id": 23316,
      "label": "intellectual disability, autosomal recessive 60",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081222",
          "GARD:0025890",
          "MEDGEN:1373351",
          "OMIM:617432",
          "UMLS:C4479476"
        ],
        "synonyms": [
          "intellectual disability, autosomal recessive 60",
          "MRT60",
          "mental retardation, autosomal recessive 60"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0044313"
    },
    {
      "id": 23651,
      "label": "intellectual disability, autosomal recessive 63",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081224",
          "GARD:0016475",
          "MEDGEN:1648348",
          "OMIM:618095",
          "UMLS:C4748167"
        ],
        "synonyms": [
          "intellectual disability, autosomal recessive 63",
          "MRT63",
          "mental retardation, autosomal recessive 63"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054861"
    },
    {
      "id": 23993,
      "label": "adenosine kinase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2861,
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111038",
          "GARD:0017321",
          "MEDGEN:1632232",
          "MESH:C567015",
          "OMIM:611094",
          "OMIM:614300",
          "Orphanet:289290",
          "UMLS:C4706555"
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        "synonyms": [
          "ADK deficiency",
          "ADK hypermethioninemia",
          "MRT8",
          "adenosine kinase deficiency",
          "autosomal recessive intellectual disability 8",
          "hypermethioninemia due to adenosine kinase deficiency",
          "hypermethioninemia encephalopathy due to ADK deficiency",
          "hypermethioninemia encephalopathy due to adenosine kinase deficiency",
          "mental retardation, autosomal recessive 8",
          "mental retardation, autosomal recessive 8, formerly",
          "mental retardation, autosomal recessive 8; MRT8"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare inborn error of metabolism characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dysfunction, hypotonia and facial dysmorphism (most significant is frontal bossing, macrocephaly, hypertelorism and depressed nasal bridge). Epileptic seizures, hypoglycemia and/or cardiac defects (pulmonary stenosis, atrial and/or ventricular septal defect, coarctation of the aorta) may be associated. Clinical picture may range from neurological symptoms only to multi-organ involvement."
      },
      "child_count": 0,
      "reference_id": "MONDO:0100255"
    },
    {
      "id": 25499,
      "label": "intellectual developmental disorder, autosomal recessive 78",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026722",
          "MEDGEN:1840905",
          "OMIM:620237",
          "UMLS:C5830269"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859373"
    },
    {
      "id": 25645,
      "label": "intellectual developmental disorder, autosomal recessive 79",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
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      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026812",
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          "OMIM:620393",
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        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957288"
    },
    {
      "id": 25791,
      "label": "intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026905",
          "MEDGEN:1850178",
          "OMIM:620653",
          "UMLS:C5882733"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957999"
    },
    {
      "id": 25876,
      "label": "intellectual developmental disorder, autosomal recessive 81",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026975",
          "MEDGEN:1844192",
          "OMIM:620700",
          "UMLS:C5882758"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0958204"
    },
    {
      "id": 25955,
      "label": "intellectual developmental disorder, autosomal recessive 82",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060947",
          "GARD:0027032",
          "MEDGEN:1858975",
          "OMIM:620779",
          "UMLS:C5935601"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0968944"
    },
    {
      "id": 26200,
      "label": "intellectual developmental disorder, autosomal recessive 83",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061114",
          "GARD:0027435",
          "MEDGEN:1876500",
          "OMIM:621100",
          "UMLS:C6012698"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0976231"
    }
  ],
  "roots": [
    {
      "id": 2962,
      "label": "non-syndromic intellectual disability"
    },
    {
      "id": 17944,
      "label": "disorder of carbohydrate transmembrane transport and absorption"
    },
    {
      "id": 24319,
      "label": "intellectual disability, autosomal recessive"
    }
  ]
}