{
    "disease_id": "DOID:0111551", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "neurogenic scapuloperoneal syndrome, Kaeser type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "scapuloperoneal syndrome, neurogenic type, of Kaeser"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "Kaeser syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "stark-Kaeser syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "scapuloperoneal syndrome, neurogenic, Kaeser type; SCPNK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "scapuloperoneal syndrome, neurogenic, Kaeser type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008407", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008407", 
            "name": "SCPNK"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111551", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111551", 
            "name": "Kaeser syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111551", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111551", 
            "name": "Stark-Kaeser syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111551", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111551", 
            "name": "scapuloperoneal syndrome type Kaeser"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111551", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111551", 
            "name": "scapuloperoneal syndrome, neurogenic, Kaeser type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111551", 
        "description": "A myopathy characterized by adult onset of foot dorsiflexor weakness, peroneal muscle weakness, scapuloperoneal weakness, and shoulder girdle muscle atrophy that has_material_basis_in heterozygous mutation in DES on chromosome 2q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111551", 
        "name": "neurogenic scapuloperoneal syndrome Kaeser type"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/181400", 
            "id": "181400", 
            "database": "MIM"
        }
    ]
}