{
    "disease_id": "DOID:0080960",
    "recommended_name": {
        "id": "DOID:0080960",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080960",
        "name": "amelogenesis imperfecta type 2A6",
        "description": "An amelogenesis imperfecta that is characterized by enamel of normal thickness that is hypomineralized and has a mottled appearance and that has_material_basis_in homozygous mutation in the G protein-coupled receptor-68 (GPR68) on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "DOID:0080960",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080960",
            "name": "Amelogenesis imperfecta, hypomaturation type, IIA6",
            "description": ""
        },
        {
            "id": "MONDO:0014971",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014971",
            "name": "amelogenesis imperfecta, hypomaturation type, IIa6",
            "description": ""
        },
        {
            "id": "MONDO:0014971",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014971",
            "name": "AI2A6",
            "description": ""
        },
        {
            "id": "MONDO:0014971",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014971",
            "name": "amelogenesis imperfecta, hypomaturation type, IIa6",
            "description": ""
        },
        {
            "id": "MONDO:0014971",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014971",
            "name": "amelogenesis imperfecta, hypomaturation type, IIa6; AI2A6",
            "description": ""
        },
        {
            "id": "MIM:617217",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617217",
            "name": "Amelogenesis imperfecta, hypomaturation type, 2A6",
            "description": "Amelogenesis imperfecta, hypomaturation type, 2A6"
        }
    ]
}