{
    "disease_id": "DOID:0110064",
    "recommended_name": {
        "id": "DOID:0110064",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110064",
        "name": "amelogenesis imperfecta type 1H",
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the integrin beta-6 gene (ITGB6) on chromosome 2q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110064",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110064",
            "name": "AI1H",
            "description": ""
        },
        {
            "id": "DOID:0110064",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110064",
            "name": "amelogenesis imperfecta type IH",
            "description": ""
        },
        {
            "id": "MONDO:0014540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014540",
            "name": "amelogenesis imperfecta type 1H",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ITGB6 gene."
        },
        {
            "id": "MONDO:0014540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014540",
            "name": "AI1H",
            "description": ""
        },
        {
            "id": "MONDO:0014540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014540",
            "name": "ITGB6 amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0014540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014540",
            "name": "amelogenesis imperfecta caused by mutation in ITGB6",
            "description": ""
        },
        {
            "id": "MONDO:0014540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014540",
            "name": "amelogenesis imperfecta, type IH",
            "description": ""
        },
        {
            "id": "MIM:616221",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616221",
            "name": "Amelogenesis imperfecta 1H",
            "description": "Amelogenesis imperfecta 1H"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110064"
    ],
    "unlinked_id_list": []
}