DISEASES

Disease-gene associations mined from literature

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 ...