{
  "id": 19033,
  "label": "angioosteohypotrophic syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019156",
  "properties": {
    "xrefs": [
      "GARD:0018927",
      "MEDGEN:1641209",
      "Orphanet:75508",
      "SCTID:765750001",
      "UMLS:C4707561"
    ],
    "synonyms": [
      "Phlebectatic osteohypoplastic angiodysplasia",
      "Servelle-Martorell syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Angioosteohypotrophic syndrome is a rare, congenital, vascular anomaly syndrome characterized by venous or, on occasion, arterial malformations which lead to soft tissue hypertrophy and bone hypoplasia. Affected limb is generally shortened, highly deformed, painful and edematous and associates bone and muscle hypotrophy. Single parts, or multiple small parts, of limbs are typically affected but more extensive involvement, including complete extremity, shoulder girdle and axilla, has been reported."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 7153,
      "label": "bone development disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7061,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080006",
          "EFO:0005541",
          "MEDGEN:2309",
          "SCTID:371521007",
          "UMLS:C0005941"
        ],
        "synonyms": [
          "bone development disease",
          "bone development disease or disorder",
          "disease of bone development",
          "disease or disorder of bone development",
          "disorder of bone development"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease involving the bone development."
      },
      "child_count": 18,
      "reference_id": "MONDO:0005497"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7153,
      "label": "bone development disease"
    }
  ]
}