{
    "disease_id": "DOID:0110052",
    "recommended_name": {
        "id": "DOID:0110052",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110052",
        "name": "amelogenesis imperfecta type 1B",
        "description": "An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110052",
            "name": "AI1B",
            "description": ""
        },
        {
            "id": "DOID:0110052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110052",
            "name": "AIH2",
            "description": ""
        },
        {
            "id": "DOID:0110052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110052",
            "name": "amelogenesis imperfecta type IB",
            "description": ""
        },
        {
            "id": "DOID:0110052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110052",
            "name": "hereditary localized enamel hypoplasia",
            "description": ""
        },
        {
            "id": "DOID:0110052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110052",
            "name": "autosomal dominant hypoplastic local amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta type 1B",
            "description": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ENAM gene."
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "AI1B",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "ENAM amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta caused by mutation in ENAM",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta caused by mutation in enam",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta type IB",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "autosomal dominant hypoplastic local amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "enam amelogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "hereditary localized enamel hypoplasia",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "AIH2",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta, hypoplastic local, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta, type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "amelogenesis imperfecta, type IB",
            "description": ""
        },
        {
            "id": "MONDO:0007092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007092",
            "name": "enamel hypoplasia, hereditary localized",
            "description": ""
        },
        {
            "id": "MIM:104500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/104500",
            "name": "Amelogenesis imperfecta 1B",
            "description": "Amelogenesis imperfecta 1B"
        }
    ]
}