All diseases

OMIM ID
256500
OMIM term:
NETHERTON SYNDROME; NETH
Alternative terms:
NS
NETHERTON DISEASE
(∗) Location:
5q32  
(†) Associated OMIM genes:
SPINK5  
(‡) Associated MGI genes:
Dsg4   Spink5  

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* quick link - http://q.sanger.ac.uk/tfa7oslo