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

2 clinical trials for this condition and its sub-types, 1 tagged with Xeroderma pigmentosum-Cockayne syndrome complex itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Hereditary photodermatosis (31)

Sub-types of Xeroderma pigmentosum-Cockayne syndrome complex

Xeroderma pigmentosum group F 1 trial
Xeroderma pigmentosum group B 0 trials
Xeroderma pigmentosum group D 0 trials
Xeroderma pigmentosum group G 0 trials
Xeroderma pigmentosum, type F/Cockayne syndrome 0 trials
Xeroderma pigmentosum, type G/Cockayne syndrome 0 trials

Including sub-types (2) Tagged with Xeroderma pigmentosum-Cockayne syndrome complex (1)

Completed 1

Scientists study rare DNA repair diseases to unlock cancer prevention secrets

Knowledge-focused Completed

This study looked at people with three rare genetic conditions—xeroderma pigmentosum (XP), Cockayne syndrome (CS), and trichothiodystrophy (TTD)—that affect the body's ability to repair DNA. Researchers examined 709 participants to understand how these defects relate to cancer ri…

Sponsor: National Cancer Institute (NCI) • Aim: Knowledge-focused

Last updated Sep 18, 2026 00:00 UTC

Xeroderma pigmentosum-Cockayne syndrome complex

Where it sits in the disease tree

Scientists study rare DNA repair diseases to unlock cancer prevention secrets