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Human Disease and Mouse Model Detail
Human Disease

Term: Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency
OMIM ID: 202010

Synonyms 11-beta-Hydroxylase Deficiency; Adrenal Hyperplasia, Hypertensive Form; Adrenal Hyperplasia IV; P450c11b1 Deficiency; Steroid 11-Beta-Hydroxylase Deficiency
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Cyp11b1 CYP11B1
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory