{
    "disease_id": "DOID:0060945",
    "recommended_name": {
        "id": "DOID:0060945",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060945",
        "name": "amelogenesis imperfecta type 1K",
        "description": "An amelogenesis imperfecta characterized by hypoplastic enamel of all teeth that has_material_basis_in heterozygous mutation in the SP6 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0031084",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031084",
            "name": "amelogenesis imperfecta, IIa 1K",
            "description": ""
        },
        {
            "id": "MONDO:0031084",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031084",
            "name": "AI1K",
            "description": ""
        },
        {
            "id": "MONDO:0031084",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031084",
            "name": "amelogenesis imperfecta, IIa 1K",
            "description": ""
        },
        {
            "id": "MONDO:0031084",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0031084",
            "name": "amelogenesis imperfecta, hypoplastic IIa 1K",
            "description": ""
        },
        {
            "id": "MIM:620104",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620104",
            "name": "Amelogenesis imperfecta 1K",
            "description": "Amelogenesis imperfecta 1K"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060945"
    ],
    "unlinked_id_list": []
}