{
  "id": 17067,
  "label": "hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016574",
  "properties": {
    "xrefs": [
      "GARD:0003347",
      "MEDGEN:371988",
      "MESH:C537836",
      "OMIM:154000",
      "Orphanet:2435",
      "SCTID:733469003",
      "UMLS:C1835172"
    ],
    "synonyms": [
      "Westerhof-Beemer-Cormane syndrome",
      "Westerhof Beemer Cormane syndrome",
      "congenital hypomelanotic and hypermelanotic macules",
      "hereditary congenital hypopigmented and hyperpigmented macules",
      "macules hereditary congenital hypopigmented and hyperpigmented",
      "macules, hereditary congenital hypopigmented and hyperpigmented"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome is a neurocutaneous syndrome characterized by congenital hypomelanotic and hypermelanotic cutaneous macules. It has been described in individuals spanning three generations of an Indian family. Some of the patients also had retarded growth and intellectual deficit."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19139,
      "label": "skin pigmentation disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10123",
          "ICD9:709.09",
          "MEDGEN:316465",
          "MESH:D010859",
          "NCIT:C34557",
          "Orphanet:79374",
          "UMLS:C1704421"
        ],
        "synonyms": [
          "pigmentation anomaly of the skin",
          "pigmentation disease of zone of skin",
          "zone of skin pigmentation disease",
          "pigmentation disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A pigmentation disease that involves the zone of skin."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019288"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19139,
      "label": "skin pigmentation disorder"
    }
  ]
}