{
  "id": 10023,
  "label": "microcephaly-albinism-digital anomalies syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008750",
  "properties": {
    "xrefs": [
      "GARD:0003604",
      "MEDGEN:395372",
      "MESH:C537322",
      "OMIM:203340",
      "Orphanet:2513",
      "SCTID:719377004",
      "UMLS:C1859910"
    ],
    "synonyms": [
      "Castro Gago-Pombo-Novo syndrome",
      "microcephaly-albinism-digital anomalies syndrome",
      "albinism-microcephaly digital anomalies syndrome",
      "albinism-microcephaly-digital anomalies syndrome"
    ],
    "definition": "Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe."
  },
  "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"
    }
  ]
}