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Human Disease and Mouse Model Detail
Human Disease Adrenal Hyperplasia, Congenital, Due to Steroid 11-Beta-Hydroxylase Deficiency
OMIM ID: 202010
Human Phenotype Ontology associations
Synonyms 11-beta-Hydroxylase Deficiency; Adrenal Hyperplasia; Adrenal Hyperplasia IV; Adrenal Hyperplasia, Hypertensive Form; P450c11b1 Deficiency; Steroid 11-Beta-Hydroxylase Deficiency
View all models View ALL (1) mouse models for this human disease.
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
     CYP11B1*, CYP11B2 Cyp11b1*, Cyp11b2 View 1 model HGNC
References Disease References using Mouse Models (1)

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