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Human Disease and Mouse Model Detail
Human Disease Hyperaldosteronism, Familial, Type I; HALD1
OMIM ID: 103900
Human Phenotype Ontology associations
Synonyms ACTH-Dependent Hyperaldosteronism Syndrome; Aldosteronism, Sensitive to Dexamethasone; FH I; Glucocorticoid-Remediable Aldosteronism; GRA; Glucocorticoid-Suppressible Hyperaldosteronism; GSH; Hyperaldosteronism, Familial
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   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
11/29/2016
MGI 6.06
The Jackson Laboratory