{
    "disease_id": "DOID:0111722",
    "recommended_name": {
        "id": "DOID:0111722",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111722",
        "name": "amelogenesis imperfecta type 3C",
        "description": "An amelogenesis imperfecta type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the RELT gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111722",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111722",
            "name": "AI3C",
            "description": ""
        },
        {
            "id": "DOID:0111722",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111722",
            "name": "amelogenesis imperfecta type IIIC",
            "description": ""
        },
        {
            "id": "DOID:0111722",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111722",
            "name": "autosomal recessive amelogenesis imperfecta hypocalcification type",
            "description": ""
        },
        {
            "id": "MIM:618386",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618386",
            "name": "Amelogenesis imperfecta 3C",
            "description": "Amelogenesis imperfecta 3C"
        }
    ]
}