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bn:01924720n
Noun Concept
Categories: Fatty-acid metabolism disorders, Autosomal recessive disorders
EN
mitochondrial trifunctional protein deficiency  MTP deficiency  TFP deficiency  TPA deficiency  trifunctional protein deficiency
EN
Mitochondrial trifunctional protein deficiency is an autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats to energy, particularly during periods without food. Wikipedia
Definitions
Relations
Sources
EN
Mitochondrial trifunctional protein deficiency is an autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats to energy, particularly during periods without food. Wikipedia
An inherited fatty acid oxidation disorder. Wikipedia Disambiguation
medical condition Wikidata
IS A
genetic disease
disease
rare disease
Inborn error of lipid metabolism
dyslipidemia
+1 relations
GENETIC ASSOCIATION
HADHA
HADHB
Wikipedia
EN
mitochondrial trifunctional protein deficiency
Wikidata
EN
Mitochondrial trifunctional protein deficiency
Wikipedia Redirections
EN
MTP deficiency, TFP deficiency, TPA deficiency, trifunctional protein deficiency, Trifunctional protein deficiency, type 2
Wikidata Alias
EN
mitochondrial trifunctional protein deficiency

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