{
    "disease_id": "DOID:0110846", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "XP, Group E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "XP-E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "XPE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "XP5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "XP group E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum, complementation group type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum group type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010213", 
            "name": "xeroderma pigmentosum, complementation group E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110846", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110846", 
            "name": "XP group E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110846", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110846", 
            "name": "XP5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110846", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110846", 
            "name": "XPE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110846", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110846", 
            "name": "xeroderma pigmentosum V"
        }, 
        {
            "url": "https://www.omim.org/entry/278740", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:278740", 
            "name": "Xeroderma pigmentosum complementation group E"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110846", 
        "description": "A xeroderma pigmentosum characterized by a mild phenotype that has_material_basis_in homozygous mutation in the DDB2 gene on chromosome 11p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110846", 
        "name": "xeroderma pigmentosum group E"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/278740", 
            "id": "278740", 
            "database": "MIM"
        }
    ]
}