All diseases

OMIM ID
113800
OMIM term:
EPIDERMOLYTIC HYPERKERATOSIS; EHK
Alternative terms:
BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ
BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; BCIE
BULLOUS ICHTHYOSIFORM ERYTHRODERMA; BIE
EPIDERMOLYTIC ICHTHYOSIS EPIDERMOLYTIC HYPERKERATOSIS, LATE-ONSET, INCLUDED
(∗) Location:
12q13.13   17q21.2  
(†) Associated OMIM genes:
KRT1   KRT10  
(‡) Associated MGI genes:
Jup   Krt10   Krt1  

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* quick link - http://q.sanger.ac.uk/f5yn49ae