All diseases

OMIM ID
308300
OMIM term:
INCONTINENTIA PIGMENTI; IP
Alternative terms:
INCONTINENTIA PIGMENTI, FAMILIAL MALE-LETHAL TYPE
BLOCH-SULZBERGER SYNDROME
INCONTINENTIA PIGMENTI, TYPE II, FORMERLY; IP2, FORMERLY
(∗) Location:
Xq28  
(†) Associated OMIM genes:
IKBKG  
(‡) Associated MGI genes:
Ikbkg  

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