Term Name:	glycogen storage disease IXa
Synonyms:	glycogen storage disease type 9A, glycogen storage disease type IXa, glycogenosis type 9A, glycogenosis type IXa, GSD type 9A, GSD type IXa, GSD9A
Definition:	A glycogen storage disease IX characterized by hepatomegaly, growth retardation, elevation of glutamate-pyruvate transaminase and glutamate-oxaloacetate transaminase, hypercholesterolemia, hypertriglyceridemia, and fasting hyperketosis, but symptoms gradually disappear with age, that has_material_basis_in X-linked inheritance of mutation in the PHKA2 gene on chromosome Xp22.
Ontology:	Human Disease [DOID:0111042]   ( DOID:0111042 )