Cure My Disease

Don't miss your cure!

 Log in / Sign up

Xeroderma pigmentosum-Cockayne syndrome complex

MONDO:0016354

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).

Also known as: XP/CS complex

9 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Xeroderma pigmentosum group F (1) Xeroderma pigmentosum group B (0) Xeroderma pigmentosum group D (0) Xeroderma pigmentosum group G (0) Xeroderma pigmentosum, type F/Cockayne syndrome (0) Xeroderma pigmentosum, type G/Cockayne syndrome (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Syndromic disease (24) Human disease (14) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Hereditary photodermatosis (0)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2
Sort by