{
    "disease_id": "DOID:0111552", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008408", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008408", 
            "name": "amyotrophy, neurogenic scapuloperoneal, New England type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008408", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008408", 
            "name": "scapuloperoneal spinal muscular atrophy; SPSMA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008408", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008408", 
            "name": "scapuloperoneal neuronopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008408", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008408", 
            "name": "neurogenic scapuloperoneal amyotrophy, New England type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008408", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008408", 
            "name": "SPSMA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111552", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111552", 
            "name": "neurogenic scapuloperoneal amyotrophy, New England type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111552", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111552", 
            "name": "SPSMA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111552", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111552", 
            "name": "scapuloperoneal neuronopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111552", 
        "description": "A motor neuron disease characterized by progressive scapuloperoneal atrophy and weakness, laryngeal palsy, congenital absence of muscles and in some cases developmental abnormalities of the bones that has_material_basis_in heterozygous mutation in TRPV4 on chromosome 12q24.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111552", 
        "name": "scapuloperoneal spinal muscular atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/181405", 
            "id": "181405", 
            "database": "MIM"
        }
    ]
}