{
    "disease_id": "DOID:0111194", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "adult-onset proximal spinal muscular atrophy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "autosomal dominant adult-onset proximal SMA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "spinal muscular atrophy, late-onset, FINKEL type; SMAFK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "spinal muscular atrophy, proximal, adult, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "Finkel disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "autosomal dominant late-onset spinal muscular atrophy, Finkel type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "SMAFK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "spinal muscular atrophy, late-onset, FINKEL type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008453", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008453", 
            "name": "Finkel late-adult type Sma"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "Finkel disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "Finkel late-adult type SMA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "SMAFK"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "autosomal dominant adult-onset proximal SMA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "autosomal dominant late-onset spinal muscular atrophy, Finkel type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111194", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111194", 
            "name": "autosomal dominant adult proximal spinal muscular atrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111194", 
        "description": "A spinal muscular atrophy characterized by adult-onset of slowly progressive, proximal muscular weakness with fasciculations and absent/hypoactive deep tendon reflexes, without bulbar or pyramidal involvement that has_material_basis_in heterozygous mutation in VAPB on 20q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111194", 
        "name": "autosomal dominant adult-onset proximal spinal muscular atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111194#disease-associations", 
            "id": "0111194", 
            "database": "Alliance of Genome Resources"
        }
    ]
}