{
    "disease_id": "DOID:0110065",
    "recommended_name": {
        "id": "DOID:0110065",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110065",
        "name": "amelogenesis imperfecta type 1F",
        "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110065",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110065",
            "name": "AI1F",
            "description": ""
        },
        {
            "id": "DOID:0110065",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110065",
            "name": "amelogenesis imperfecta hypoplastic type IF",
            "description": ""
        },
        {
            "id": "DOID:0110065",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110065",
            "name": "amelogenesis imperfecta type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta type 1F",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the AMBN gene."
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta, type IF; AI1F",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta hypoplastic type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "AI1F",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta caused by mutation in AMBN",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta, type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "AMBN amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta, hypoplastic type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0014560",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014560",
            "name": "amelogenesis imperfecta, type 1F",
            "description": ""
        },
        {
            "id": "MIM:616270",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616270",
            "name": "Amelogenesis imperfecta 1F",
            "description": "Amelogenesis imperfecta 1F"
        }
    ]
}