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bn:01324624n
Noun Concept
Categories: X-linked recessive disorders, Articles with short description, Rare syndromes
EN
FG syndrome  Fg Syndrome 1  FG syndrome type 1  Keller syndrome  Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of Corpus Callosum
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
Definitions
Relations
Sources
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
Disease Wikidata
IS A
rare disease
syndrome
GENETIC ASSOCIATION
FLNA
CASK
MED12
NAMED AFTER
John M. Opitz
Wikipedia
EN
FG syndrome
Wikidata
EN
FG syndrome
Wikipedia Redirections
EN
Opitz-Kaveggia syndrome, Opitz–Kaveggia syndrome
Wikidata Alias
EN
Fg Syndrome, Fg Syndrome 1, FG syndrome type 1, Keller syndrome, Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of Corpus Callosum, OKS, Opitz-Kaveggia syndrome, OPITZ-KAVEGGIA SYNDROME; OKS, Opitz–Kaveggia syndrome

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