Xeroderma pigmentosum-Cockayne syndrome complex

rare

Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome (CS).

Identifiers: MONDO:0016354 Orphanet:220295
Part of: Hereditary photodermatosis Syndromic disease
Also known as: XP/CS complex

Subtypes

All diseases Rare only

Disease	ID	Genes
Xeroderma pigmentosum group B	MONDO:0012531	ERCC3
Xeroderma pigmentosum group D	MONDO:0010212	ERCC2
Xeroderma pigmentosum group F	MONDO:0010215	ERCC4
Xeroderma pigmentosum group G	MONDO:0010216	ERCC5
Xeroderma pigmentosum, type F/Cockayne syndrome	MONDO:0800313
Xeroderma pigmentosum, type G/Cockayne syndrome	MONDO:0800314

Rare disease

Projects

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