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- Glycogen_storage_disease_type_I abstract "Glycogen storage disease type I (GSD I) or von Gierke's disease, is the most common of the glycogen storage diseases. This genetic disease results from deficiency of the enzyme glucose-6-phosphatase, and has an incidence in the American population of approximately 1 in 50,000 to 100,000 births.The deficiency impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis. Since these are the two principal metabolic mechanisms by which the liver supplies glucose to the rest of the body during periods of fasting, it causes severe hypoglycemia and results in increased glycogen storage in liver and kidneys. This can lead to enlargement of both. Both organs function normally in childhood, but are susceptible to a variety of problems in adult years. Other metabolic derangements include lactic acidosis and hyperlipidemia. Frequent or continuous feedings of cornstarch or other carbohydrates are the principal treatment. Other therapeutic measures may be needed for associated problems.The disease was named after Edgar von Gierke, the German doctor who discovered it.".
- Glycogen_storage_disease_type_I diseasesdb "5284".
- Glycogen_storage_disease_type_I emedicineSubject "ped".
- Glycogen_storage_disease_type_I emedicineTopic "2416".
- Glycogen_storage_disease_type_I icd10 "E74.0".
- Glycogen_storage_disease_type_I icd9 "271.0".
- Glycogen_storage_disease_type_I medlineplus "000338".
- Glycogen_storage_disease_type_I omim "232200".
- Glycogen_storage_disease_type_I thumbnail Autorecessive.svg?width=300.
- Glycogen_storage_disease_type_I wikiPageExternalLink NBK1312.
- Glycogen_storage_disease_type_I wikiPageID "1716876".
- Glycogen_storage_disease_type_I wikiPageRevisionID "600743003".
- Glycogen_storage_disease_type_I diseasesdb "5284".
- Glycogen_storage_disease_type_I emedicinesubj "ped".
- Glycogen_storage_disease_type_I emedicinetopic "2416".
- Glycogen_storage_disease_type_I genereviewsname "Glycogen Storage Disease Type I".
- Glycogen_storage_disease_type_I genereviewsnbk "NBK1312".
- Glycogen_storage_disease_type_I hasPhotoCollection Glycogen_storage_disease_type_I.
- Glycogen_storage_disease_type_I icd "271".
- Glycogen_storage_disease_type_I icd "E74.0".
- Glycogen_storage_disease_type_I medlineplus "338".
- Glycogen_storage_disease_type_I name "Glycogen storage disease type I".
- Glycogen_storage_disease_type_I omim "232200".
- Glycogen_storage_disease_type_I wordnet_type synset-disease-noun-1.
- Glycogen_storage_disease_type_I subject Category:Autosomal_recessive_disorders.
- Glycogen_storage_disease_type_I subject Category:Hepatology.
- Glycogen_storage_disease_type_I subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Glycogen_storage_disease_type_I type Abstraction100002137.
- Glycogen_storage_disease_type_I type Act100030358.
- Glycogen_storage_disease_type_I type Attribute100024264.
- Glycogen_storage_disease_type_I type AutosomalRecessiveDisorders.
- Glycogen_storage_disease_type_I type Condition113920835.
- Glycogen_storage_disease_type_I type Disease114070360.
- Glycogen_storage_disease_type_I type Disorder114052403.
- Glycogen_storage_disease_type_I type Event100029378.
- Glycogen_storage_disease_type_I type IllHealth114052046.
- Glycogen_storage_disease_type_I type Illness114061805.
- Glycogen_storage_disease_type_I type InbornErrorsOfCarbohydrateMetabolism.
- Glycogen_storage_disease_type_I type Mistake100070965.
- Glycogen_storage_disease_type_I type Nonaccomplishment100066216.
- Glycogen_storage_disease_type_I type PathologicalState114051917.
- Glycogen_storage_disease_type_I type PhysicalCondition114034177.
- Glycogen_storage_disease_type_I type PsychologicalFeature100023100.
- Glycogen_storage_disease_type_I type State100024720.
- Glycogen_storage_disease_type_I type YagoPermanentlyLocatedEntity.
- Glycogen_storage_disease_type_I type Disease.
- Glycogen_storage_disease_type_I type AilmentCondition.
- Glycogen_storage_disease_type_I type Situation.
- Glycogen_storage_disease_type_I comment "Glycogen storage disease type I (GSD I) or von Gierke's disease, is the most common of the glycogen storage diseases. This genetic disease results from deficiency of the enzyme glucose-6-phosphatase, and has an incidence in the American population of approximately 1 in 50,000 to 100,000 births.The deficiency impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis.".
- Glycogen_storage_disease_type_I label "Choroba von Gierkego".
- Glycogen_storage_disease_type_I label "Doença de Von Gierke".
- Glycogen_storage_disease_type_I label "Enfermedad de Von Gierke".
- Glycogen_storage_disease_type_I label "Glycogen storage disease type I".
- Glycogen_storage_disease_type_I label "Glycogénose type 1".
- Glycogen_storage_disease_type_I label "Malattia di von Gierke".
- Glycogen_storage_disease_type_I label "Von-Gierke-Krankheit".
- Glycogen_storage_disease_type_I label "Болезнь Гирке".
- Glycogen_storage_disease_type_I sameAs Von-Gierke-Krankheit.
- Glycogen_storage_disease_type_I sameAs Enfermedad_de_Von_Gierke.
- Glycogen_storage_disease_type_I sameAs Glycogénose_type_1.
- Glycogen_storage_disease_type_I sameAs Malattia_di_von_Gierke.
- Glycogen_storage_disease_type_I sameAs Choroba_von_Gierkego.
- Glycogen_storage_disease_type_I sameAs Doença_de_Von_Gierke.
- Glycogen_storage_disease_type_I sameAs m.05qr5l.
- Glycogen_storage_disease_type_I sameAs Q630090.
- Glycogen_storage_disease_type_I sameAs Q630090.
- Glycogen_storage_disease_type_I sameAs Glycogen_storage_disease_type_I.
- Glycogen_storage_disease_type_I wasDerivedFrom Glycogen_storage_disease_type_I?oldid=600743003.
- Glycogen_storage_disease_type_I depiction Autorecessive.svg.
- Glycogen_storage_disease_type_I isPrimaryTopicOf Glycogen_storage_disease_type_I.
- Glycogen_storage_disease_type_I name "Glycogen storage disease type I".
