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bn:01606575n
Noun Concept
SYL
No term available
EN
Barth syndrome is a rare but serious X-linked genetic disorder, caused by changes in phospholipid structure and metabolism. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
mitochondrial myopathy
EN
3-methylglutaconic aciduria
EN
dyslipidemia
GENETIC ASSOCIATION
EN
tafazzin
HEALTH SPECIALTY
EN
endocrinology
SYMPTOMS
EN
agranulocytosis
EN
cardiac arrhythmia
EN
clubfoot
EN
heart failure
EN
fatigue
+18 relations

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