{
  "id": 22992,
  "label": "glycosylphosphatidylinositol biosynthesis defect 16",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0040500",
  "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3146",
          "GARD:0021314",
          "ICD9:272.8",
          "ICD9:272.9",
          "MEDGEN:57587",
          "MedDRA:10061227",
          "NCIT:C97092",
          "Orphanet:309005",
          "SCTID:267431006",
          "SCTID:402788005",
          "UMLS:C0154251"
        ],
        "synonyms": [
          "disorder of lipid metabolism",
          "dyslipidaemia",
          "dyslipidemia",
          "lipid metabolism disorder",
          "fatty acid metabolism disorder"
        ],
        "definition": "An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production."
      },
      "child_count": 29,
      "reference_id": "MONDO:0002525"
    },
    {
      "id": 19320,
      "label": "autosomal recessive non-syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2962,
        17944,
        24319
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 204,
      "reference_id": "MONDO:0019502"
    },
    {
      "id": 21353,
      "label": "disorder of GPI anchor biosynthesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6795,
        21354
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "GPI anchor biosynthetic process disease",
          "GPIBD",
          "disorder of GPI anchor biosynthetic process",
          "glycosylphosphatidylinositol biosynthesis defect"
        ],
        "definition": "A disease that has its basis in the disruption of GPI anchor biosynthetic process."
      },
      "child_count": 22,
      "reference_id": "MONDO:0024321"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder"
    },
    {
      "id": 19320,
      "label": "autosomal recessive non-syndromic intellectual disability"
    },
    {
      "id": 21353,
      "label": "disorder of GPI anchor biosynthesis"
    }
  ]
}