All diseases

OMIM ID
601675
OMIM term:
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE; TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
Alternative terms:
TAY SYNDROME, INCLUDED
TRICHOTHIODYSTROPHY WITH CONGENITAL ICHTHYOSIS, INCLUDED
ICHTHYOSIS, CONGENITAL, WITH TRICHOTHIODYSTROPHY, INCLUDED
IBIDS SYNDROME, INCLUDED
(∗) Location:
19q13.32   2q14.3   6q25.3  
(†) Associated OMIM genes:
ERCC2   ERCC3   GTF2H5  
(‡) Associated MGI genes:
Ercc2   Xpa  

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