{
    "disease_id": "DOID:0090002", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "albinism-deafness of Tietz"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "hypopigmentation/deafness of Tietz"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "Tietz albinism-deafness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "TADS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "hypopigmentation-deafness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007077", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007077", 
            "name": "Tietz albinism-deafness syndrome; TADS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090002", 
            "name": "Tietz albinism-deafness syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090002", 
            "name": "albinism-deafness of Tietz"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090002", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090002", 
            "name": "hypopigmentation/deafness of Tietz"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090002", 
        "description": "A syndrome that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that has_material_basis_in mutation in the MITF gene on chromosome 3p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090002", 
        "name": "Tietz syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090002#disease-associations", 
            "id": "0090002", 
            "database": "Alliance of Genome Resources"
        }
    ]
}