{
    "disease_id": "DOID:0050473", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008763", 
            "name": "Alss"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008763", 
            "name": "alms"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008763", 
            "name": "Alstrom's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008763", 
            "name": "Alstrom syndrome; alms"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008763", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008763", 
            "name": "Alstrm syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050473", 
        "description": "A syndrome that is characterized by multiorgan dysfunction. The key features are childhood obesity, blindness due to congenital retinal dystrophy, and sensorineural hearing loss with autosomal recessive inheritance and has_material_basis_in mutations in the ALMS1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050473", 
        "name": "Alstrom syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/203800", 
            "id": "203800", 
            "database": "MIM"
        }
    ]
}