{
  "id": 25961,
  "label": "hypocalcified amelogenesis imperfecta",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0968955",
  "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"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 19324,
      "label": "amelogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5879
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:0828-0533",
          "DOID:2187",
          "GARD:0005791",
          "ICD9:520.5",
          "MEDGEN:240",
          "MESH:D000567",
          "NORD:765",
          "OMIMPS:104500",
          "Orphanet:88661",
          "SCTID:78494001",
          "UMLS:C0002452",
          "icd11.foundation:1923123066"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body."
      },
      "child_count": 14,
      "reference_id": "MONDO:0019507"
    }
  ],
  "children": [
    {
      "id": 8919,
      "label": "amelogenesis imperfecta, type 3A",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25961
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007538"
    },
    {
      "id": 20662,
      "label": "amelogenesis imperfecta type 3B",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25961
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080243",
          "GARD:0018258",
          "MEDGEN:1621302",
          "OMIM:617607",
          "UMLS:C4539891"
        ],
        "synonyms": [
          "AI3B",
          "amelogenesis imperfecta, type 3B",
          "amelogenesis imperfecta, type IIIB"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0021547"
    },
    {
      "id": 22384,
      "label": "amelogenesis imperfecta, type 3C",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25961
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111722",
          "GARD:0025728",
          "MEDGEN:1676410",
          "OMIM:618386",
          "UMLS:C5193069"
        ],
        "synonyms": [
          "AI3C",
          "AMELOGENESIS IMPERFECTA, TYPE IIIC",
          "Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032717"
    }
  ],
  "roots": [
    {
      "id": 19324,
      "label": "amelogenesis imperfecta"
    }
  ]
}