Search Ontology:
Human Disease

cortisone reductase deficiency 2

Term ID
DOID:0090140
Synonyms
  • CORTRD2
Definition
A cortisone reductase deficiency that is characterized by a failure to regenerate cortisol via the enzyme 11-beta-hydroxysteroid dehydrogenase, resulting in ACTH-mediated adrenal hyperandrogenism, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the 11-beta-hydroxysteroid dehydrogenase type I (HSD11B1) gene on chromosome 1q32. (2)
References
Ontology
Human Disease   ( DOID:0090140 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations