pyruvate decarboxylase deficiency

Summary
Synonym
  • deficiency of pyruvic dehydrogenase
  • pyruvate dehydrogenase complex deficiency disease
  • pyruvate dehydrogenase deficiency
Definition
A carbohydrate metabolic disorder characterized by the buildup of lactic acid in the body and a variety of neurological problems and caused by a deficiency of one of the three enzymes in the pyruvate dehydrogenase complex.
Super Class
carbohydrate metabolic disorder
External Links
Related Genes
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
5162 PDHB pyruvate dehydrogenase E1 subunit beta
8050 PDHX pyruvate dehydrogenase complex component X
56994 CHPT1 choline phosphotransferase 1
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
Displaying all 4 entries
Gene ID Gene Symbol Description Source
18597 Pdha1 pyruvate dehydrogenase E1 alpha 1
18598 Pdha2 pyruvate dehydrogenase E1 alpha 2
68263 Pdhb pyruvate dehydrogenase (lipoamide) beta
235339 Dlat dihydrolipoamide S-acetyltransferase
Displaying all 3 entries
Gene ID Gene Symbol Description Source
81654 Dlat dihydrolipoamide S-acetyltransferase
117098 Pdha2 pyruvate dehydrogenase E1 subunit alpha 2
289950 Pdhb pyruvate dehydrogenase E1 subunit beta
The Human Phenotype Ontology
Displaying entries 101 - 110 of 149 in total
HPO ID HPO Term
HP:0000639 Nystagmus
HP:0000657 Oculomotor apraxia
HP:0001256 Intellectual disability, mild
HP:0001266 Choreoathetosis
HP:0001270 Motor delay
HP:0001319 Neonatal hypotonia
HP:0001347 Hyperreflexia
HP:0001348 Brisk reflexes
HP:0002194 Delayed gross motor development
HP:0002307 Drooling
Displaying all 4 entries
Gene ID Gene Symbol Description
8050 PDHX pyruvate dehydrogenase complex component X
5162 PDHB pyruvate dehydrogenase E1 subunit beta
1737 DLAT dihydrolipoamide S-acetyltransferase
5160 PDHA1 pyruvate dehydrogenase E1 subunit alpha 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024