MeSH Browser

MeSH Supplementary: 18-Hydroxylase deficiency
Unique ID: C537806
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537806
Entry Term(s): 18-Oxidase Deficiency; 18-alpha hydroxylase deficiency; Aldosterone Deficiency Type I; Aldosterone Deficiency Type II; Aldosterone deficiency 1; Aldosterone deficiency due to defect in 18-hydroxylase; CMO I Deficiency; CMO II Deficiency; Corticosterone Methyloxidase Type I Deficiency; Corticosterone Methyloxidase Type II Deficiency; Corticosterone methyloxidase type 1 deficiency; Hyperreninemic Hypoaldosteronism, Familial, Type I; Steroid 18-Hydroxylase Deficiency; Steroid 18-Oxidase Deficiency
Registry Number: 0
Heading Mapped to: *Hypoaldosteronism; Cytochrome P-450 CYP11B2 / *deficiency
Frequency: 8
Date of Entry: 2010/06/25
Revision Date: 2013/11/06

18-Hydroxylase deficiency MeSH Supplementary Concept Data 2024