Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0080156 - X-linked adrenal hypoplasia congenita

Disease Ontology Definition:An adrenal cortical hypofunction that is characterized by a reduction in adrenal gland function resulting from incomplete development of the adrenal cortex and has_material_basis_in the nuclear receptor NR0B1 (DAX1) gene.

Synonyms: congenital adrenal hypoplasia

Xenbase Genes : nr0b1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010264 - X-linked adrenal hypoplasia congenita

MIM:
MIM:300200 - ADRENAL HYPOPLASIA, CONGENITAL; AHC

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): adrenal cortical hypofunction (is_a), X-linked recessive disease (is_a)