{
  "id": 10595,
  "label": "hydrocephaly-tall stature-joint laxity syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009363",
  "properties": {
    "xrefs": [
      "GARD:0001666",
      "MEDGEN:383828",
      "MESH:C535770",
      "OMIM:236660",
      "Orphanet:2181",
      "SCTID:732926009",
      "UMLS:C1856051"
    ],
    "synonyms": [
      "Daish-Hardman-Lamont syndrome",
      "Daish Hardman Lamont syndrome",
      "hydrocephalus, tall stature, JOINT laxity, and kyphoscoliosis",
      "hydrocephalus, tall stature, joint laxity and kyphoscoliosis",
      "hydrocephaly - tall stature - joint laxity"
    ],
    "definition": "Hydrocephaly-tall stature-joint laxity syndrome is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019833",
          "MEDGEN:1842829",
          "Orphanet:102285",
          "UMLS:C5680373"
        ],
        "synonyms": [
          "MCA without intellectual disability",
          "multiple congenital anomalies without intellectual disability with or without dysmorphism"
        ]
      },
      "child_count": 168,
      "reference_id": "MONDO:0015161"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    }
  ]
}