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- Glycogen_storage_disease_type_XI abstract "Glycogen storage disease type XI is a form of glycogen storage disease.It is also known as "Fanconi–Bickel syndrome", for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated with GLUT2, a glucose transport protein which, when functioning normally, allows glucose to exit several tissues, including the liver, nephrons,and enterocytes of the intestines, and enter the blood. The syndrome results in hepatomegaly secondary to glycogen accumulation, glucose and galactose intolerance, fasting hypoglycaemia, a characteristic proximal tubular nephropathy and severe short stature.".
- Glycogen_storage_disease_type_XI diseasesdb "31709".
- Glycogen_storage_disease_type_XI omim "227810".
- Glycogen_storage_disease_type_XI wikiPageID "17107822".
- Glycogen_storage_disease_type_XI wikiPageRevisionID "604245752".
- Glycogen_storage_disease_type_XI diseasesdb "31709".
- Glycogen_storage_disease_type_XI hasPhotoCollection Glycogen_storage_disease_type_XI.
- Glycogen_storage_disease_type_XI name "Glycogen storage disease type XI".
- Glycogen_storage_disease_type_XI omim "227810".
- Glycogen_storage_disease_type_XI wordnet_type synset-disease-noun-1.
- Glycogen_storage_disease_type_XI subject Category:Hepatology.
- Glycogen_storage_disease_type_XI subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Glycogen_storage_disease_type_XI subject Category:Muscular_disorders.
- Glycogen_storage_disease_type_XI type Abstraction100002137.
- Glycogen_storage_disease_type_XI type Act100030358.
- Glycogen_storage_disease_type_XI type Attribute100024264.
- Glycogen_storage_disease_type_XI type Condition113920835.
- Glycogen_storage_disease_type_XI type Disease114070360.
- Glycogen_storage_disease_type_XI type Disorder114052403.
- Glycogen_storage_disease_type_XI type Event100029378.
- Glycogen_storage_disease_type_XI type IllHealth114052046.
- Glycogen_storage_disease_type_XI type Illness114061805.
- Glycogen_storage_disease_type_XI type InbornErrorsOfCarbohydrateMetabolism.
- Glycogen_storage_disease_type_XI type InbornErrorsOfMetabolism.
- Glycogen_storage_disease_type_XI type Mistake100070965.
- Glycogen_storage_disease_type_XI type MuscularDisorders.
- Glycogen_storage_disease_type_XI type Nonaccomplishment100066216.
- Glycogen_storage_disease_type_XI type PathologicalState114051917.
- Glycogen_storage_disease_type_XI type PhysicalCondition114034177.
- Glycogen_storage_disease_type_XI type PsychologicalFeature100023100.
- Glycogen_storage_disease_type_XI type State100024720.
- Glycogen_storage_disease_type_XI type YagoPermanentlyLocatedEntity.
- Glycogen_storage_disease_type_XI type Disease.
- Glycogen_storage_disease_type_XI type AilmentCondition.
- Glycogen_storage_disease_type_XI type Situation.
- Glycogen_storage_disease_type_XI comment "Glycogen storage disease type XI is a form of glycogen storage disease.It is also known as "Fanconi–Bickel syndrome", for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated with GLUT2, a glucose transport protein which, when functioning normally, allows glucose to exit several tissues, including the liver, nephrons,and enterocytes of the intestines, and enter the blood.".
- Glycogen_storage_disease_type_XI label "Glycogen storage disease type XI".
- Glycogen_storage_disease_type_XI label "Zespół Fanconiego-Bickela".
- Glycogen_storage_disease_type_XI sameAs Sindrom_Fanconi-Bickel.
- Glycogen_storage_disease_type_XI sameAs Zespół_Fanconiego-Bickela.
- Glycogen_storage_disease_type_XI sameAs m.042167h.
- Glycogen_storage_disease_type_XI sameAs Q5572613.
- Glycogen_storage_disease_type_XI sameAs Q5572613.
- Glycogen_storage_disease_type_XI sameAs 395.
- Glycogen_storage_disease_type_XI sameAs Glycogen_storage_disease_type_XI.
- Glycogen_storage_disease_type_XI wasDerivedFrom Glycogen_storage_disease_type_XI?oldid=604245752.
- Glycogen_storage_disease_type_XI isPrimaryTopicOf Glycogen_storage_disease_type_XI.
- Glycogen_storage_disease_type_XI name "Glycogen storage disease type XI".