{
    "disease_id": "DOID:0080953",
    "recommended_name": {
        "id": "DOID:0080953",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080953",
        "name": "amelogenesis imperfecta type 1J",
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ACPT on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0080953",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080953",
            "name": "Amelogenesis imperfecta, type IJ",
            "description": ""
        },
        {
            "id": "MONDO:0015008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015008",
            "name": "amelogenesis imperfecta, type 1J",
            "description": ""
        },
        {
            "id": "MONDO:0015008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015008",
            "name": "amelogenesis imperfecta, type 1J",
            "description": ""
        },
        {
            "id": "MONDO:0015008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015008",
            "name": "amelogenesis imperfecta, type Ij",
            "description": ""
        },
        {
            "id": "MONDO:0015008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0015008",
            "name": "AI1J",
            "description": ""
        },
        {
            "id": "MIM:617297",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617297",
            "name": "Amelogenesis imperfecta 1J",
            "description": "Amelogenesis imperfecta 1J"
        }
    ]
}