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Xeroderma pigmentosum group F

MONDO:0010215

Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC4 gene.

Also known as: ERCC4 xeroderma pigmentosum, XP, group F, XP-F, XP6, XPF, xeroderma pigmentosum caused by mutation in ERCC4, xeroderma pigmentosum group F, xeroderma pigmentosum group type F

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

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Skin disorder (132) Inborn errors of metabolism (45) Syndromic disease (25) Human disease (14) DNA repair disease (13) Hereditary skin disorder (6) Xeroderma pigmentosum (4)
Trials to join now! 2 Not yet finished but already full! 1 Completed 1
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