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 )
Other Pages
Genes Involved
Zebrafish Models