{
  "id": 8919,
  "label": "amelogenesis imperfecta, type 3A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007538",
  "properties": {
    "xrefs": [
      "DOID:0110055",
      "GARD:0024562",
      "MEDGEN:1854533",
      "MESH:C562880",
      "OMIM:130900",
      "SCTID:109471001",
      "UMLS:C5886770"
    ],
    "synonyms": [
      "amelogenesis imperfecta hypomineralization type",
      "amelogenesis imperfecta type 3",
      "amelogenesis imperfecta type III",
      "ADHCAI",
      "AI3",
      "FAM83H amelogenesis imperfecta",
      "amelogenesis imperfecta caused by mutation in FAM83H",
      "amelogenesis imperfecta, type 3A",
      "AI3A",
      "amelogenesis imperfecta type 3A",
      "amelogenesis imperfecta, hypocalcification type, autosomal dominant",
      "amelogenesis imperfecta, hypomineralization type",
      "amelogenesis imperfecta, type 3",
      "amelogenesis imperfecta, type III",
      "amelogenesis imperfecta, type IIIA"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25961,
      "label": "hypocalcified amelogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016931",
          "MEDGEN:140773",
          "Orphanet:100032",
          "UMLS:C0399376",
          "icd11.foundation:1793262466"
        ],
        "synonyms": [
          "amelogenesis imperfecta type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0968955"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25961,
      "label": "hypocalcified amelogenesis imperfecta"
    }
  ]
}