{
  "id": 9984,
  "label": "Goodman syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008711",
  "properties": {
    "xrefs": [
      "GARD:0002549",
      "MEDGEN:78551",
      "MESH:C537287",
      "OMIM:201020",
      "Orphanet:65798",
      "SCTID:720600004",
      "UMLS:C0265303"
    ],
    "synonyms": [
      "ACPS 4",
      "ACPS4",
      "Goodman syndrome",
      "acrocephalopolysyndactyly type 4",
      "Goodman camptodactyly",
      "acrocephalopolysyndactyly type IV"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Goodman syndrome is an extremely rare genetic disorder characterized by marked malformations of the head and face (essentially acrocephaly), abnormalities of the hands and feet (polydactyly, syndactyly, clinodactyly, camptodactyly, ulnar deviation), and congenital heart disease. There have been no further descriptions in the literature since 1979. Goodman syndrome could be a variant of Carpenter syndrome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2717,
      "label": "acrocephalopolysyndactyly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19539
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022707",
          "MEDGEN:673840",
          "SCTID:205260006",
          "UMLS:C0687154"
        ],
        "synonyms": [
          "ACPS"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A common presentation of craniosynostosis and polysyndactyly."
      },
      "child_count": 4,
      "reference_id": "MONDO:0000078"
    },
    {
      "id": 16088,
      "label": "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025062",
          "Orphanet:102284"
        ],
        "synonyms": [
          "MCA/variable MR",
          "multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome"
        ]
      },
      "child_count": 69,
      "reference_id": "MONDO:0015160"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2717,
      "label": "acrocephalopolysyndactyly"
    },
    {
      "id": 16088,
      "label": "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome"
    }
  ]
}