All diseases

OMIM ID
612132
OMIM term:
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT
Alternative terms:

(∗) Location:
14q13.2  
(†) Associated OMIM genes:
NFKBIA  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/o1r19fcz