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bn:03544046n
Noun Concept
Categories: Autosomal recessive disorders, Inborn errors of carbohydrate metabolism
EN
pyruvate carboxylase deficiency  pyruvate carboxylase deficiency disease  Ataxia with Lactic Acidosis, Type II  Ataxia With Lactic Acidosis 2  Ataxia with lactic acidosis type 2
EN
Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid to accumulate in the blood. Wikipedia
Definitions
Relations
Sources
EN
Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid to accumulate in the blood. Wikipedia
Human disease Wikidata
IS A
genetic disease
rare disease
Inborn errors of carbohydrate metabolism
GENETIC ASSOCIATION
pyruvate carboxylase
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
pyruvate carboxylase deficiency
Wikidata
EN
pyruvate carboxylase deficiency disease
Wikipedia Redirections
EN
Ataxia with Lactic Acidosis, Type II, Deficiency of pyruvate carboxylase, PC deficiency, Pyruvate carboxylase deficiency disease
Wikidata Alias
EN
Ataxia With Lactic Acidosis 2, Ataxia with lactic acidosis type 2, Ataxia with lactic acidosis type II, deficiency of pyruvic carboxylase, Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency, Leigh syndrome due to PC deficiency, Leigh Syndrome Due to Pyruvate Carboxylase Deficiency, Pc Deficiency, PYRUVATE CARBOXYLASE DEFICIENCY

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