Glycogen storage disease type IX

Property	Value
rdf:type	owl:NamedIndividual Genetic disease or disorder
rdfs:label	Glycogen storage disease type IX
owl:sameAs	dbr:Glycogen_storage_disease_type_IX
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Glycogen_storage_disease http://en.wikipedia.org/wiki/Category:Genetic_diseases_and_disorders http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_inheritance http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_mechanism http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_system
skos:prefLabel	Glycogen storage disease type IX
skos:altLabel	GSD IX GSD type IX glycogen storage disease type IX
clgo:geneReviewsId	55061
clgo:geneReviewsName	Phosphorylase Kinase Deficiency
clgo:icd10	E74.09
clgo:medicalCause	PHKB PHKA2 Phosphorylase kinase, alpha 1
clgo:medicalDiagnosis	Urinalysis
clgo:omim	306000
clgo:symptom	Hepatomegaly

About: clgr:Glycogen_storage_disease_type_IX