All diseases

OMIM ID
278730
OMIM term:
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD
Alternative terms:
XP, GROUP D; XPDC
XERODERMA PIGMENTOSUM IV; XP4 TRICHOTHIODYSTROPHY WITH SUN SENSITIVITY, INCLUDED
TRICHOTHIODYSTROPHY, TYPE 1, INCLUDED; TTD1, INCLUDED
XERODERMA PIGMENTOSUM VIII, FORMERLY; XP8, FORMERLY
XP, GROUP H, FORMERLY; XPH, FORMERLY
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
ERCC2  
(‡) Associated MGI genes:
Ercc2  

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