{
    "disease_id": "DOID:0111722", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111722", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111722", 
            "name": "AI3C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111722", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111722", 
            "name": "amelogenesis imperfecta type IIIC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111722", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111722", 
            "name": "autosomal recessive amelogenesis imperfecta hypocalcification type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111722", 
        "description": "An amelogenesis imperfecta type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the RELT gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111722", 
        "name": "amelogenesis imperfecta type 3C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111722#disease-associations", 
            "id": "0111722", 
            "database": "Alliance of Genome Resources"
        }
    ]
}