Disease #03665 (PHA2B (pseudohypoaldosteronism type 2B (PHA-2B)), OMIM:614491)

Official abbreviation PHA2B
Name pseudohypoaldosteronism type 2B (PHA-2B)
OMIM ID 614491
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WNK4
Associated tissues -
Disease features -
Remarks -