{
    "disease_id": "DOID:0051080",
    "recommended_name": {
        "id": "DOID:0051080",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051080",
        "name": "Alport syndrome 3B",
        "description": "An Alport syndrome that is characterized by glomerular basement membrane abnormalities and that has_material_basis_in homozygous or compound heterozygous mutation in the COL4A3 gene on chromosome 2q36. Sensorineural hearing loss and ocular manifestations may be present."
    },
    "synonyms": [
        {
            "id": "MONDO:0957811",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957811",
            "name": "Alport syndrome 3b, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:620536",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620536",
            "name": "Alport syndrome 3B, autosomal recessive",
            "description": "Alport syndrome 3B, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051080"
    ],
    "unlinked_id_list": []
}