corticosterone methyloxidase type 1 deficiency
MONDO:0008751Mondo
Findings
No curated finding names corticosterone methyloxidase type 1 deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CYP11B2HGNC:2592
- Definitive · Natera · Autosomal recessive · 2023
- Moderate · Ambry Genetics · Autosomal recessive · 2018
Where it sits
Other names
2 names
Resolves to: corticosterone methyloxidase type 1 deficiency
- Also called
- corticosterone 18-monooxygenase deficiencyhypoaldosteronism, congenital, due to cmo i deficiency