Cure My Disease

Don't miss your cure!

Log in / Sign up

Glycogen storage disease IXc

MONDO:0013091

A liver PhK deficiency caused by variants in the PHKG2 gene

Also known as: GSD type 9C, GSD type IXc, GSD9C, PHKG2 glycogen storage disease, PHKG2-related glycogen storage disease type IX, glycogen storage disease IXc, glycogen storage disease caused by mutation in PHKG2, glycogen storage disease type IXc

3 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Liver disorder (307) Metabolic disease (233) Hereditary disease (176) Digestive system disorder (160) Endocrine system disorder (72) Inborn errors of metabolism (45) Disorder of glycogen metabolism (14) Human disease (14) Hepatobiliary disorder (10)

Trials to join now! 2 Not yet finished but already full! 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC