Disease #00738 (HOKPP2 (paralysis, hypokalemic, periodic, type 2 (HOKPP-2)), OMIM:613345)

Official abbreviation HOKPP2
Name paralysis, hypokalemic, periodic, type 2 (HOKPP-2)
OMIM ID 613345
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 SCN4A
Associated tissues -
Disease features autosomal dominant
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.