{
    "disease_id": "DOID:0080243",
    "recommended_name": {
        "id": "DOID:0080243",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080243",
        "name": "amelogenesis imperfecta type 3B",
        "description": "An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0021547",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021547",
            "name": "amelogenesis imperfecta type 3B",
            "description": ""
        },
        {
            "id": "MONDO:0021547",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021547",
            "name": "AI3B",
            "description": ""
        },
        {
            "id": "MONDO:0021547",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021547",
            "name": "amelogenesis imperfecta, type 3B",
            "description": ""
        },
        {
            "id": "MONDO:0021547",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021547",
            "name": "amelogenesis imperfecta, type IIIB",
            "description": ""
        },
        {
            "id": "MIM:617607",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617607",
            "name": "Amelogenesis imperfecta 3B",
            "description": "Amelogenesis imperfecta 3B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080243"
    ],
    "unlinked_id_list": []
}