{
    "disease_id": "DOID:0110055",
    "recommended_name": {
        "id": "DOID:0110055",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110055",
        "name": "amelogenesis imperfecta type 3A",
        "description": "An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110055",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110055",
            "name": "ADHCAI",
            "description": ""
        },
        {
            "id": "DOID:0110055",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110055",
            "name": "AI3",
            "description": ""
        },
        {
            "id": "DOID:0110055",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110055",
            "name": "amelogenesis imperfecta hypomineralization type",
            "description": ""
        },
        {
            "id": "DOID:0110055",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110055",
            "name": "amelogenesis imperfecta type III",
            "description": ""
        },
        {
            "id": "DOID:0110055",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110055",
            "name": "autosomal dominant amelogenesis imperfecta hypocalcification type",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type 3A",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene."
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "autosomal dominant amelogenesis imperfecta hypocalcification type",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type III",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta caused by mutation in FAM83H",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "AI3",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "FAM83H amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type IIIA; AI3A",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, hypocalcification type, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta type 3A",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta hypomineralization type",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "AI3A",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type 3A",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, type III; AI3",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta type III",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "ADHCAI",
            "description": ""
        },
        {
            "id": "MONDO:0007538",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007538",
            "name": "amelogenesis imperfecta, hypomineralization type",
            "description": ""
        },
        {
            "id": "MIM:130900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/130900",
            "name": "Amelogenesis imperfecta 3A",
            "description": "Amelogenesis imperfecta 3A"
        }
    ]
}