All diseases

OMIM ID
609796
OMIM term:
PEELING SKIN SYNDROME, ACRAL TYPE
Alternative terms:
PEELING SKIN SYNDROME, TYPE A
ACRAL PEELING SKIN SYNDROME; APSS
(∗) Location:
15q15.2  
(†) Associated OMIM genes:
TGM5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/r922to4f