All diseases

OMIM ID
242100
OMIM term:
ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1; NCIE1
Alternative terms:
IECN1
ICHTHYOSIFORM ERYTHRODERMA, BROCQ CONGENITAL, NONBULLOUS FORM
NONBULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA 1
NCIE
CIE
(∗) Location:
14q12   17p13.1  
(†) Associated OMIM genes:
ALOX12B   ALOXE3   TGM1  
(‡) Associated MGI genes:
Alox12b  

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