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bn:01324624n
Noun Concept
SYL
No term available
EN
FG syndrome is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. Wikipedia
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Sources
IS A
EN
rare disease
EN
syndrome
GENETIC ASSOCIATION
EN
FLNA
EN
CASK
EN
MED12
NAMED AFTER
John Marius Opitz

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