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bn:01924720n
Noun Concept
JA
No term available
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
Relations
Sources
IS A
遺伝子疾患
病気
希少疾患
先天性脂質代謝異常症
脂質代謝障害
+1 relations
GENETIC ASSOCIATION
長鎖-3-ヒドロキシアシルCoAデヒドロゲナーゼ
EN
HADHB

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