{
    "disease_id": "DOID:0060283", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "peeling skin syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "deciduous skin"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "CDSN peeling skin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "skin peeling, familial continuous generalized"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "PSS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "peeling skin syndrome 1; PSS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "PSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "peeling skin syndrome caused by mutation in CDSN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024548", 
            "name": "keratolysis exfoliativa congenita"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060283", 
        "description": "A skin disease that is characterized by the painless peeling of the top layer of skin predominately on the hands and feet, has_material_basis_in autosomal recessive inheritance of mutation in the TGM5 gene and/pr CSTA gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060283", 
        "name": "peeling skin syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060283#disease-associations", 
            "id": "0060283", 
            "database": "Alliance of Genome Resources"
        }
    ]
}