Xeroderma pigmentosum group G

Definition

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC5 gene.

Also known as ERCC5 xeroderma pigmentosum, xeroderma pigmentosum caused by mutation in ERCC5, xeroderma pigmentosum group G, xeroderma pigmentosum group type G, xeroderma pigmentosum, complementation group type G, xeroderma pigmentosum, group G, xeroderma pigmentosum, group G/Cockayne syndrome, XP-G, XP7, XPG — per MONDO

Also identified as

• DOID 0110849 per MONDO
• MESH C562593 per MONDO
• NCIT C3969 per MONDO
• OMIM 278780 per MONDO
• Orphanet 276267 per MONDO
• SCTID 36454001 per MONDO
• UMLS C0268141 per MONDO

Affected Organs