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Human Disease

familial hyperaldosteronism III

Term ID
DOID:0061248
Synonyms
Definition
A familial hyperaldosteronism characterized by hypertension secondary to massive adrenal mineralocorticoid production that has_material_basis_in heterozygous mutation in the KCNJ5 gene on chromosome 11q24. https://pubmed.ncbi.nlm.nih.gov/18505761/
References
Ontology
Human Disease   ( DOID:0061248 )
Relationships
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Genes Involved
Zebrafish Models