{
    "disease_id": "DOID:0060161", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "Kennedy disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinal and bulbar muscular atrophy, X-linked 1; SMAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinal and bulbar muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "Kennedy spinal and bulbar muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "bulbospinal neuronopathy, X-linked recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "SMAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "SBMA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinal and bulbar muscular atrophy, X-linked 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "X-linked BSMA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinal and bulbar muscular atrophy, X-linked type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinobulbar muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "X-linked spinal and bulbar muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "X-linked bulbo-spinal atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "X-linked bulbospinal amyotrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "X-linked bulbospinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "spinal bulbar muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010735", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010735", 
            "name": "bulbospinal muscular atrophy, X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "Kennedy disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "SBMA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "Spinobulbar Muscular Atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "X-Linked Bulbo-Spinal Atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "X-linked Spinal and Bulbar Muscular Atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060161", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060161", 
            "name": "spinal bulbar muscular atrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060161", 
        "description": "A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060161", 
        "name": "Kennedy's disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060161#disease-associations", 
            "id": "0060161", 
            "database": "Alliance of Genome Resources"
        }
    ]
}