Xeroderma pigmentosum, type G/Cockayne syndrome
MONDO:0800314Also known as: XPG/CS
0 clinical trials for this condition and its sub-types.
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Disease
(717)
Hereditary disease
(188)
Skin disorder
(135)
Syndromic disease
(25)
Human disease
(15)
Hereditary skin disorder
(7)
Disease of genetic or genomic mechanism
(2)
Xeroderma pigmentosum-Cockayne syndrome complex
(1)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)
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