Human genes for xeroderma pigmentosum group A
Xeroderma pigmentosum group A [DOID:0110843]
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: xeroderma pigmentosum group A, DOID:0110843, xeroderma pigmentosum group As, xeroderma pigmentosum 1, xeroderma pigmentosum complementation group A ...