Glycogen storage disease type I

Property	Value
rdf:type	owl:NamedIndividual Primary immunodeficiency Autosomal recessive disorder MeSH code (C18) Inborn error of carbohydrate metabolism
rdfs:label	Glycogen storage disease type I
owl:sameAs	dbr:Glycogen_storage_disease_type_I
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/List_of_primary_immunodeficiencies http://en.wikipedia.org/wiki/Medical_genetics_of_Jews http://en.wikipedia.org/wiki/Category:Inborn_errors_of_carbohydrate_metabolism http://en.wikipedia.org/wiki/Human_genome http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C18)
skos:prefLabel	Glycogen storage disease type I
skos:altLabel	type I GSD I GSD type I Glycogen Storage Disease type 1a Glycogen storage disease type 1b Glycogen_storage_disease_type_I glycogen storage disease type I von Gierke's disease
clgo:complications	Lactic acidosis,hyperlipidemia,non-alcoholic fatty liver disease,hepatocellular adenoma,inflammatory bowel disease
clgo:diseasesDB	5284
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	2416
clgo:geneReviewsId	NBK1312
clgo:geneReviewsName	Glycogen Storage Disease Type I
clgo:icd10	E74.0
clgo:icd9	271.0
clgo:medicalCause	Human genetics
clgo:medicalDiagnosis	Genetic testing Hypoglycemia Hepatomegaly Neutropenia
clgo:medication	Filgrastim
clgo:medlinePlus	000338
clgo:omim	232200
clgo:treatment	Diet (nutrition) Corn starch

About: clgr:Glycogen_storage_disease_type_I