{
    "disease_id": "DOID:0060283",
    "recommended_name": {
        "id": "DOID:0060283",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060283",
        "name": "peeling skin syndrome",
        "description": "A skin disease that is characterized by the painless, continuous peeling of the top layer of skin."
    },
    "synonyms": [
        {
            "id": "DOID:0060283",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060283",
            "name": "deciduous skin",
            "description": ""
        },
        {
            "id": "DOID:0060283",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060283",
            "name": "familial continuous skin peeling syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060283",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060283",
            "name": "keratosis exfoliativa congenita",
            "description": ""
        },
        {
            "id": "DOID:0060283",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060283",
            "name": "peeling skin disease",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "peeling skin syndrome 1",
            "description": "Any peeling skin syndrome in which the cause of the disease is a mutation in the CDSN gene."
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "CDSN peeling skin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "PSS type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "generalised deciduous skin type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "generalised peeling skin syndrome type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "generalized deciduous skin type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "generalized peeling skin syndrome type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "inflammatory peeling skin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "peeling skin syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "peeling skin syndrome caused by mutation in CDSN",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "peeling skin syndrome type B",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "PSS",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "PSS1",
            "description": ""
        },
        {
            "id": "MONDO:0024548",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "name": "skin peeling, familial continuous generalised",
            "description": ""
        },
        {
            "id": "MIM:270300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270300",
            "name": "Peeling skin syndrome 1",
            "description": "Peeling skin syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0070520",
            "label": "peeling skin syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070521",
            "label": "peeling skin syndrome 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070523",
            "label": "peeling skin syndrome 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070524",
            "label": "peeling skin syndrome 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070525",
            "label": "peeling skin syndrome 6",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070520",
        "DOID:0070524",
        "DOID:0070525",
        "DOID:0060283",
        "DOID:0070523",
        "DOID:0070521"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0060283",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060283",
            "categories": []
        },
        {
            "id": "MONDO:0024548",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024548",
            "categories": []
        },
        {
            "id": "MIM:270300",
            "database": "MIM",
            "url": "https://www.omim.org/entry/270300",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q15517-1",
            "uniprot_ac": "Q15517",
            "uniprot_id": "CDSN_HUMAN",
            "refseq_ac": "",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Corneodesmosin",
                    "type": "recommended"
                },
                {
                    "name": "S protein",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "CDSN",
                    "type": "recommended"
                }
            ],
            "record_id": "Q15517-1",
            "evidence": [
                {
                    "id": "270300",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/270300"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0060283"
}