{
  "id": 16555,
  "label": "autosomal dominant non-syndromic intellectual disability",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015802",
  "properties": {
    "xrefs": [
      "DOID:0060307",
      "GARD:0012107",
      "MEDGEN:1826082",
      "Orphanet:178469",
      "UMLS:C5680502"
    ],
    "synonyms": [
      "autosomal dominant mental retardation",
      "autosomal dominant non-syndromic intellectual disability",
      "non-syndromic intellectual disability, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Autosomal dominant form of non-syndromic intellectual disability."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 26,
  "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": 23914,
      "label": "intellectual disability, autosomal dominant",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        3324,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:156200"
        ],
        "synonyms": [
          "mental retardation, autosomal dominant",
          "autosomal dominant intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 87,
      "reference_id": "MONDO:0100172"
    }
  ],
  "children": [
    {
      "id": 13909,
      "label": "intellectual disability, autosomal dominant 22",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070052",
          "GARD:0024892",
          "MESH:C567346",
          "OMIM:612337"
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        "synonyms": [
          "MRD22",
          "ZBTB18 autosomal dominant non-syndromic intellectual disability",
          "autosomal dominant intellectual disability 22",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18",
          "intellectual disability, autosomal dominant 22",
          "intellectual disability, autosomal dominant type 22",
          "mental retardation, autosomal dominant type 22",
          "autosomal dominant non-syndromic intellectual disability 22",
          "chromosome 1Q43-q44 deletion syndrome",
          "chromosome 1Qter deletion syndrome",
          "mental retardation, autosomal dominant 22"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the ZBTB18 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012869"
    },
    {
      "id": 14302,
      "label": "neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070050",
          "GARD:0024910",
          "MEDGEN:462050",
          "NORD:2013",
          "OMIM:613443",
          "Orphanet:664410",
          "UMLS:C3150700"
        ],
        "synonyms": [
          "MEF2C Deficiency",
          "MEF2C autosomal dominant non-syndromic intellectual disability",
          "MEF2C haploinsufficiency syndrome (MCHS)",
          "MEF2C-related neurodevelopmental disorder",
          "MEF2C-related syndrome",
          "MRD20",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in MEF2C",
          "intellectual disability, autosomal dominant 20",
          "intellectual disability, autosomal dominant type 20",
          "mental retardation, autosomal dominant 20",
          "mental retardation, autosomal dominant type 20",
          "neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language",
          "intellectual disability, stereotypic movements, epilepsy, and/or cerebral malformations",
          "mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MEF2C gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013266"
    },
    {
      "id": 15578,
      "label": "intellectual disability, autosomal dominant 33",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070063",
          "GARD:0016082",
          "MEDGEN:899389",
          "OMIM:616311",
          "UMLS:C4225375"
        ],
        "synonyms": [
          "DPP6 autosomal dominant non-syndromic intellectual disability",
          "MRD33",
          "autosomal dominant intellectual disability 33",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6",
          "intellectual disability, autosomal dominant 33",
          "intellectual disability, autosomal dominant type 33",
          "mental retardation, autosomal dominant type 33",
          "autosomal dominant non-syndromic intellectual disability 33",
          "mental retardation, autosomal dominant 33"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014580"
    },
    {
      "id": 15597,
      "label": "intellectual disability, autosomal dominant 34",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070064",
          "GARD:0025006",
          "MEDGEN:907277",
          "OMIM:616351",
          "UMLS:C4225156"
        ],
        "synonyms": [
          "COL4A3BP autosomal dominant non-syndromic intellectual disability",
          "MRD34",
          "autosomal dominant intellectual disability 34",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in COL4A3BP",
          "intellectual developmental disorder, autosomal dominant 34",
          "intellectual disability, autosomal dominant 34",
          "intellectual disability, autosomal dominant type 34",
          "mental retardation, autosomal dominant type 34",
          "autosomal dominant non-syndromic intellectual disability 34",
          "mental retardation, autosomal dominant 34"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the COL4A3BP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014599"
    },
    {
      "id": 15826,
      "label": "intellectual disability, autosomal dominant 41",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070071",
          "GARD:0025023",
          "MEDGEN:934751",
          "OMIM:616944",
          "UMLS:C4310784"
        ],
        "synonyms": [
          "MRD41",
          "TBL1XR1 autosomal dominant non-syndromic intellectual disability",
          "autosomal dominant intellectual disability 41",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1",
          "intellectual disability, autosomal dominant 41",
          "intellectual disability, autosomal dominant type 41",
          "mental retardation, autosomal dominant 41",
          "mental retardation, autosomal dominant type 41",
          "autosomal dominant non-syndromic intellectual disability 41"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014842"
    },
    {
      "id": 15840,
      "label": "intellectual disability, autosomal dominant 43",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070073",
          "GARD:0013179",
          "MEDGEN:1640004",
          "OMIM:616977",
          "SCTID:765434008",
          "UMLS:C4707429"
        ],
        "synonyms": [
          "HIVEP2 autosomal dominant non-syndromic intellectual disability",
          "MRD43",
          "autosomal dominant intellectual disability 43",
          "autosomal dominant non-syndromic intellectual disability caused by mutation in HIVEP2",
          "intellectual disability, autosomal dominant 43",
          "intellectual disability, autosomal dominant type 43",
          "mental retardation, autosomal dominant 43",
          "mental retardation, autosomal dominant type 43",
          "HIVEP2-related intellectual disability",
          "autosomal dominant intellectual disability-43",
          "autosomal dominant non-syndromic intellectual disability 43"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the HIVEP2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014858"
    },
    {
      "id": 20228,
      "label": "intellectual disability, autosomal dominant 58",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061032",
          "GARD:0016476",
          "MEDGEN:1648488",
          "OMIM:618106",
          "UMLS:C4748195"
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        "synonyms": [
          "MENTAL RETARDATION, autosomal dominant 58",
          "MRD58"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020847"
    },
    {
      "id": 22115,
      "label": "intellectual disability, autosomal dominant 45",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080236",
          "GARD:0025658",
          "MEDGEN:1616472",
          "OMIM:617600",
          "UMLS:C4539848"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 45",
          "MRD45",
          "autosomal dominant intellectual disability 45",
          "autosomal dominant mental retardation 45",
          "mental retardation, autosomal dominant 45"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030910"
    },
    {
      "id": 22116,
      "label": "intellectual disability, autosomal dominant 46",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080237",
          "GARD:0025659",
          "MEDGEN:1618560",
          "OMIM:617601",
          "UMLS:C4539851"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 46",
          "MRD46",
          "autosomal dominant intellectual disability 46",
          "autosomal dominant mental retardation 46",
          "mental retardation, autosomal dominant 46"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030911"
    },
    {
      "id": 22117,
      "label": "intellectual disability, autosomal dominant 47",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4427,
        16087,
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080238",
          "GARD:0017935",
          "MEDGEN:1622196",
          "OMIM:617635",
          "Orphanet:502434",
          "UMLS:C4539951"
        ],
        "synonyms": [
          "STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome",
          "intellectual disability, autosomal dominant 47",
          "MRD47",
          "autosomal dominant intellectual disability 47",
          "autosomal dominant mental retardation 47",
          "mental retardation, autosomal dominant 47"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030912"
    },
    {
      "id": 22119,
      "label": "Clark-Baraitser syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080234",
          "GARD:0009994",
          "MEDGEN:443983",
          "MESH:C536208",
          "OMIM:300602",
          "OMIM:617752",
          "Orphanet:600731",
          "UMLS:C2931130"
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        "synonyms": [
          "Clark-Baraitser syndrome",
          "MRD49",
          "intellectual disability, autosomal dominant 49",
          "Baraitser syndrome",
          "autosomal dominant intellectual disability 49",
          "autosomal dominant mental retardation 49",
          "intellectual disability, tall stature, obesity, macrocephaly and typical facial features",
          "mental retardation, autosomal dominant 49",
          "mental retardation, tall stature, obesity, macrocephaly and typical facial features"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030914"
    },
    {
      "id": 22121,
      "label": "intellectual disability, autosomal dominant 50",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080233",
          "GARD:0025661",
          "MEDGEN:1616989",
          "OMIM:617787",
          "UMLS:C4540470"
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        "synonyms": [
          "intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities",
          "intellectual developmental disorder, autosomal dominant 50, with behavioural abnormalities",
          "intellectual disability, autosomal dominant 50",
          "MRD50",
          "autosomal dominant intellectual disability 50",
          "autosomal dominant mental retardation 50",
          "mental retardation, autosomal dominant 50"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030916"
    },
    {
      "id": 22122,
      "label": "intellectual disability, autosomal dominant 51",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080232",
          "GARD:0025662",
          "MEDGEN:1625009",
          "OMIM:617788",
          "Orphanet:684226",
          "UMLS:C4540474"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 51",
          "MRD51",
          "autosomal dominant intellectual disability 51",
          "autosomal dominant mental retardation 51",
          "mental retardation, autosomal dominant 51"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030917"
    },
    {
      "id": 22123,
      "label": "intellectual disability, autosomal dominant 52",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080231",
          "EFO:0009152",
          "GARD:0016472",
          "MEDGEN:1615839",
          "OMIM:617796",
          "UMLS:C4540478"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 52",
          "MRD52",
          "autosomal dominant intellectual disability 52",
          "autosomal dominant mental retardation 52",
          "mental retardation, autosomal dominant 52"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030918"
    },
    {
      "id": 22124,
      "label": "intellectual disability, autosomal dominant 53",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080228",
          "EFO:0009165",
          "GARD:0016473",
          "MEDGEN:1623344",
          "OMIM:617798",
          "UMLS:C4540481"
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        "synonyms": [
          "intellectual disability, autosomal dominant 53",
          "MRD53",
          "autosomal dominant intellectual disability 53",
          "autosomal dominant mental retardation 53",
          "mental retardation, autosomal dominant 53"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030919"
    },
    {
      "id": 22125,
      "label": "intellectual disability, autosomal dominant 54",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080230",
          "GARD:0016474",
          "MEDGEN:1614787",
          "OMIM:617799",
          "UMLS:C4540484"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 54",
          "MRD54",
          "autosomal dominant intellectual disability 54",
          "autosomal dominant mental retardation 54",
          "mental retardation, autosomal dominant 54"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030920"
    },
    {
      "id": 22126,
      "label": "intellectual disability, autosomal dominant 55, with seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080227",
          "GARD:0016260",
          "MEDGEN:1635938",
          "OMIM:617831",
          "UMLS:C4693371"
        ],
        "synonyms": [
          "intellectual disability, autosomal dominant 55, with seizures",
          "MRD55",
          "autosomal dominant intellectual disability 55",
          "autosomal dominant mental retardation 55",
          "mental retardation, autosomal dominant 55, with seizures"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030921"
    },
    {
      "id": 22127,
      "label": "intellectual disability, autosomal dominant 56",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080226",
          "GARD:0013524",
          "MEDGEN:1638835",
          "OMIM:617854",
          "UMLS:C4693389"
        ],
        "synonyms": [
          "CLTC-related ID",
          "CLTC-related disorder",
          "CLTC-related intellectual disability",
          "intellectual disability, autosomal dominant 56",
          "MRD56",
          "autosomal dominant intellectual disability 56",
          "autosomal dominant mental retardation 56",
          "mental retardation, autosomal dominant 56"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030922"
    },
    {
      "id": 22253,
      "label": "intellectual developmental disorder 61",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "GARD:0018514",
          "MEDGEN:1684867",
          "OMIM:618009",
          "UMLS:C5231400"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER 61",
          "MRD61",
          "Mental Retardation, Autosomal Dominant 61"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032485"
    },
    {
      "id": 22452,
      "label": "intellectual developmental disorder 59",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061033",
          "GARD:0025746",
          "MEDGEN:1678593",
          "OMIM:618522",
          "UMLS:C5193190"
        ],
        "synonyms": [
          "intellectual developmental disorder 59",
          "INTELLECTUAL DEVELOPMENTAL DISORDER 59",
          "MRD59",
          "Mental Retardation, Autosomal Dominant 59"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032795"
    },
    {
      "id": 22480,
      "label": "intellectual developmental disorder 60 with seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "GARD:0016367",
          "MEDGEN:1684702",
          "OMIM:618587",
          "UMLS:C5231497"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER 60 WITH SEIZURES",
          "MRD60",
          "Mental Retardation, Autosomal Dominant 60, With Seizures"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032823"
    },
    {
      "id": 22571,
      "label": "intellectual developmental disorder 62",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "GARD:0025775",
          "ICD10CM:QA0.0142",
          "MEDGEN:1712636",
          "OMIM:618793",
          "UMLS:C5394083"
        ],
        "synonyms": [
          "DLG4 synaptopathy",
          "DLG4-related synaptopathy",
          "SHINE syndrome",
          "autosomal dominant intellectual developmental disorder-62",
          "intellectual developmental disorder, autosomal dominant 62",
          "sleep disturbances, hypotonia, intellectual disability, neurologic disorder, and epilepsy syndrome",
          "MRD62",
          "Mental Retardation, Autosomal Dominant 62"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032919"
    },
    {
      "id": 22590,
      "label": "intellectual developmental disorder, autosomal dominant 63, with macrocephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061036",
          "GARD:0025781",
          "MEDGEN:1716581",
          "OMIM:618825",
          "UMLS:C5394205"
        ],
        "synonyms": [
          "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY",
          "MRD63",
          "Mental Retardation, Autosomal Dominant 63, With Macrocephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032939"
    },
    {
      "id": 22664,
      "label": "Coffin-Siris syndrome 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555,
        24515
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080297",
          "GARD:0016254",
          "MEDGEN:1615540",
          "OMIM:617808",
          "UMLS:C4540499"
        ],
        "synonyms": [
          "ARID2-related BAFopathy",
          "Coffin-Siris syndrome 6",
          "COFFIN-SIRIS syndrome 6",
          "CSS6"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0033492"
    },
    {
      "id": 23639,
      "label": "intellectual disability, autosomal dominant 57",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061031",
          "GARD:0025982",
          "MEDGEN:1648280",
          "OMIM:618050",
          "UMLS:C4748003"
        ],
        "synonyms": [
          "TLK2-Related Neurodevelopmental Disorder",
          "TLK2-related neurodevelopmental disorder",
          "TLK2-related syndrome",
          "intellectual developmental disorder, autosomal dominant 57",
          "intellectual disability, autosomal dominant 57",
          "MRD57",
          "mental retardation, autosomal dominant 57"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054837"
    },
    {
      "id": 25708,
      "label": "intellectual developmental disorder, autosomal dominant 73",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16555
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061046",
          "GARD:0026856",
          "MEDGEN:1841272",
          "OMIM:620450",
          "UMLS:C5830636"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957536"
    }
  ],
  "roots": [
    {
      "id": 2962,
      "label": "non-syndromic intellectual disability"
    },
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant"
    }
  ]
}