Search Ontology:
Human Disease

familial hyperaldosteronism IV

Term ID
DOID:0061250
Synonyms
Definition
A familial hyperaldosteronism that has_material_basis_in heterozygous mutation in the CACNA1H gene on chromosome 16p13. https://pubmed.ncbi.nlm.nih.gov/25907736/
References
Ontology
Human Disease   ( DOID:0061250 )
Relationships
Other Pages
Genes Involved
Zebrafish Models