All diseases

OMIM ID
300200
OMIM term:
ADRENAL HYPOPLASIA, CONGENITAL; AHC
Alternative terms:
ADRENAL HYPOPLASIA, CONGENITAL, WITH HYPOGONADOTROPIC HYPOGONADISM; AHCH
ADDISON DISEASE, X-LINKED; AHX
AHC WITH HHG
CYTOMEGALIC ADRENOCORTICAL HYPOPLASIA
AHC WITH ISOLATED GONADOTROPIN DEFICIENCY ADRENAL HYPOPLASIA, CONGENITAL, WITH PRECOCIOUS PUBERTY, INCLUDED
ADRENAL INSUFFICIENCY, PROGRESSIVE, AND HYPOGONADOTROPIC HYPOGONADISM, INCLUDED
MINERALOCORTICOID DEFICIENCY, ISOLATED, INCLUDED
(∗) Location:
Xp21.2  
(†) Associated OMIM genes:
NR0B1  
(‡) Associated MGI genes:
Nr0b1  

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