{
    "disease_id": "DOID:0110843",
    "recommended_name": {
        "id": "DOID:0110843",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110843",
        "name": "xeroderma pigmentosum group A",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110843",
            "name": "XP group A",
            "description": ""
        },
        {
            "id": "DOID:0110843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110843",
            "name": "XP1",
            "description": ""
        },
        {
            "id": "DOID:0110843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110843",
            "name": "XPA",
            "description": ""
        },
        {
            "id": "DOID:0110843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110843",
            "name": "xeroderma pigmentosum 1",
            "description": ""
        },
        {
            "id": "DOID:0110843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110843",
            "name": "xeroderma pigmentosum complementation group A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum group A",
            "description": "Any xeroderma pigmentosum in which the cause of the disease is a mutation in the XPA gene."
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "XP-A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "XP1",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "XPA",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "XPA xeroderma pigmentosum",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum 1",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum caused by mutation in XPA",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum group A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum group type A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum, complementation group type a",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum, group A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum, complementation group A",
            "description": ""
        },
        {
            "id": "MONDO:0010210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010210",
            "name": "xeroderma pigmentosum, type 1",
            "description": ""
        },
        {
            "id": "MIM:278700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/278700",
            "name": "Xeroderma pigmentosum complementation group A",
            "description": "Xeroderma pigmentosum complementation group A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110843"
    ],
    "unlinked_id_list": []
}