{
    "disease_id": "DOID:0110843", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum, complementation group type a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum, complementation group A; XPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum group type A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XPA xeroderma pigmentosum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XP group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XP, group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum caused by mutation in XPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum, complementation group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "xeroderma pigmentosum complementation group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010210", 
            "name": "XP-A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110843", 
            "name": "XP group A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110843", 
            "name": "XP1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110843", 
            "name": "XPA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110843", 
            "name": "xeroderma pigmentosum 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110843", 
            "name": "xeroderma pigmentosum complementation group A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110843", 
        "description": "A xeroderma pigmentosum characterized by involvement of the central and peripheral nervous systems in addition to cutaneous lesions that has_material_basis_in caused by homozygous or compound heterozygous mutation in the XPA gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110843", 
        "name": "xeroderma pigmentosum group A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110843#disease-associations", 
            "id": "0110843", 
            "database": "Alliance of Genome Resources"
        }
    ]
}