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- Glycogen_storage_disease_type_0 abstract "Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme. Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is often classified with the Glycogen storage diseases because it is another defect of glycogen storage and can cause similar problems. Mutations in the liver isoform, GYS2, causes fasting hypoglycemia, high blood ketones, increased free fatty acids and low levels of alanine and lactate. Conversely, feeding in these patients results in hyperglycemia and hyperlactatemia. There are two versions: the muscle version involves GYS1 and the liver version involves GYS2.".
- Glycogen_storage_disease_type_0 diseasesdb "31944".
- Glycogen_storage_disease_type_0 emedicineSubject "ped".
- Glycogen_storage_disease_type_0 emedicineTopic "873".
- Glycogen_storage_disease_type_0 omim "240600".
- Glycogen_storage_disease_type_0 wikiPageID "2975468".
- Glycogen_storage_disease_type_0 wikiPageRevisionID "591478448".
- Glycogen_storage_disease_type_0 diseasesdb "31944".
- Glycogen_storage_disease_type_0 emedicinesubj "ped".
- Glycogen_storage_disease_type_0 emedicinetopic "873".
- Glycogen_storage_disease_type_0 hasPhotoCollection Glycogen_storage_disease_type_0.
- Glycogen_storage_disease_type_0 name "Glycogen storage disease type 0".
- Glycogen_storage_disease_type_0 omim "240600".
- Glycogen_storage_disease_type_0 wordnet_type synset-disease-noun-1.
- Glycogen_storage_disease_type_0 subject Category:Hepatology.
- Glycogen_storage_disease_type_0 subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Glycogen_storage_disease_type_0 type Disease.
- Glycogen_storage_disease_type_0 type AilmentCondition.
- Glycogen_storage_disease_type_0 type Situation.
- Glycogen_storage_disease_type_0 comment "Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme. Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is often classified with the Glycogen storage diseases because it is another defect of glycogen storage and can cause similar problems. Mutations in the liver isoform, GYS2, causes fasting hypoglycemia, high blood ketones, increased free fatty acids and low levels of alanine and lactate.".
- Glycogen_storage_disease_type_0 label "Glycogen storage disease type 0".
- Glycogen_storage_disease_type_0 sameAs m.08h4p0.
- Glycogen_storage_disease_type_0 sameAs Q5572606.
- Glycogen_storage_disease_type_0 sameAs Q5572606.
- Glycogen_storage_disease_type_0 wasDerivedFrom Glycogen_storage_disease_type_0?oldid=591478448.
- Glycogen_storage_disease_type_0 isPrimaryTopicOf Glycogen_storage_disease_type_0.
- Glycogen_storage_disease_type_0 name "Glycogen storage disease type 0".