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