corticosterone methyloxidase type 1 deficiency
Go to external page http://purl.obolibrary.org/obo/MONDO_0008751
This is just here as a test because I lose it
Term information
database
cross reference
- OMIM:203400 (MONDO:equivalentTo)
- UMLS:CN074214 (MONDO:ncbi_mim2gene_medline)
- GARD:0005660 (MONDO:equivalentTo)
- SCTID:47757001 (MONDO:equivalentTo)
- DOID:0080626 (MONDO:equivalentTo)
Subsets
gard_rare
exactMatch
- http://purl.obolibrary.org/obo/DOID_0080626
- http://linkedlifedata.com/resource/umls/id/CN074214
- https://omim.org/entry/203400
- http://identifiers.org/snomedct/47757001
has exact synonym
- corticosterone methyloxidase type 1 deficiency
- hypoaldosteronism, congenital, due to cmo i deficiency
- corticosterone 18-monooxygenase deficiency
has related synonym
- 18-hydroxycorticosterone dehydrogenase deficiency
- aldosterone deficiency due to defect in steroid 18-Hydroxylase
- CMO I deficiency
- corticosterone methyl oxidase type I deficiency
- 18-Hydroxylase deficiency
- CAH - 18-hydroxylase deficiency
- aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency
- aldosterone deficiency due to 18-hydroxylase defect
- corticosterone methyl oxidase type II deficiency
- aldosterone deficiency 1
- aldosterone deficiency due to defect in 18 hydroxylase
- steroid 18-hydroxylase deficiency
- hyperreninemic hypoaldosteronism, familial, 1
- 18-hydroxylase deficiency
- CMO 1 deficiency
- CMO II deficiency
- 18 Hydroxylase deficiency
- corticosterone methyloxidase type I deficiency
- 18 alpha hydroxylase deficiency
id
- MONDO:0008751
seeAlso
- https://github.com/monarch-initiative/mondo/issues/4521
- https://rarediseases.info.nih.gov/diseases/5660/18-hydroxylase-deficiency