{
  "id": 8449,
  "label": "autosomal dominant Aarskog syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007030",
  "properties": {
    "xrefs": [
      "DOID:0111825",
      "GARD:0015029",
      "MEDGEN:460570",
      "NORD:702",
      "OMIM:100050",
      "UMLS:C3149220"
    ],
    "synonyms": [
      "Aarskog Syndrome",
      "Aarskog syndrome",
      "Aarskog syndrome, autosomal dominant",
      "Aarskog-Scott syndrome",
      "faciogenital dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 20261,
      "label": "faciodigitogenital syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111824",
          "GARD:0004775",
          "MedDRA:10067148",
          "Orphanet:915"
        ],
        "synonyms": [
          "Aarskog syndrome",
          "Aarskog-Scott syndrome",
          "faciogenital dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. This includes X-linked, AR and AD forms of Aarskog syndrome."
      },
      "child_count": 3,
      "reference_id": "MONDO:0021005"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 20261,
      "label": "faciodigitogenital syndrome"
    }
  ]
}