{
  "id": 10592,
  "label": "hydrocephalus, nonsyndromic, autosomal recessive 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009360",
  "properties": {
    "xrefs": [
      "GARD:0024663",
      "MEDGEN:854455",
      "OMIM:236600",
      "UMLS:C3887608"
    ],
    "synonyms": [
      "CCDC88C congenital hydrocephalus",
      "congenital hydrocephalus caused by mutation in CCDC88C",
      "hydrocephalus, congenital, 1",
      "hydrocephalus, nonsyndromic, autosomal recessive 1",
      "hydrocephalus, nonsyndromic, autosomal recessive type 1",
      "HYC1",
      "hydrocephaly",
      "ventriculomegaly"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any congenital hydrocephalus in which the cause of the disease is a mutation in the CCDC88C gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "id": 16885,
      "label": "congenital hydrocephalus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3395,
        4427,
        20383,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006682",
          "ICD10CM:Q03",
          "ICD10WHO:Q03",
          "MEDGEN:9336",
          "MedDRA:10010506",
          "NANDO:2200822",
          "NCIT:C98876",
          "OMIMPS:236600",
          "Orphanet:2185",
          "SCTID:47032000",
          "UMLS:C0020256",
          "icd11.foundation:1878746673"
        ],
        "synonyms": [
          "congenital hydrocephalus",
          "HYC3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hydrocephalus that is present at birth."
      },
      "child_count": 32,
      "reference_id": "MONDO:0016349"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 16885,
      "label": "congenital hydrocephalus"
    }
  ]
}