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Human Disease and Mouse Model Detail
Human Disease Corticosterone Methyloxidase Type I Deficiency
OMIM ID: 203400
Human Phenotype Ontology associations
Synonyms 18-hydroxylase Deficiency; Aldosterone Deficiency Due to Defect in Steroid 18-Hydroxylase; Aldosterone Deficiency I; CMO I Deficiency; Corticosterone Methyloxidase Deficiency; Hyperreninemic Hypoaldosteronism, Familial, 1; FHHA1A; Steroid 18-hydroxylase Deficiency
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     CYP11B2*, CYP11B1 Cyp11b1, Cyp11b2   HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory