{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "hemorrhagic familial nephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "ATS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "congenital hereditary hematuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "Alport syndrome, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "nephropathy and deafness, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "hemorrhagic hereditary nephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010520", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010520", 
            "name": "Alport syndrome, X-linked; ATS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110034", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110034", 
            "name": "nephropathy and deafness, X-linked"
        }, 
        {
            "url": "https://www.omim.org/entry/301050", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:301050", 
            "name": "Alport syndrome 1, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110034", 
        "description": "An Alport syndrome that has_material_basis_in mutation in the gene encoding the alpha-5 chain of basement membrane collagen type IV (COL4A5).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110034", 
        "name": "X-linked Alport syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/301050", 
            "id": "301050", 
            "database": "MIM"
        }
    ]
}