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bn:03272993n
Noun Concept
Categories: Transcription factor deficiencies, Syndromes with dysmelia, Syndromes affecting head size, Rare syndromes, Autosomal dominant disorders
EN
Greig cephalopolysyndactyly syndrome  cephalopolysyndactyly syndrome  GCPS  Greig cephalopolysyndactyly  Greig cephalopolysyndactyly (GCPS) syndrome
EN
Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. Wikipedia
Definitions
Relations
Sources
EN
Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. Wikipedia
Acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face Wikidata
IS A
rare disease
genetic disease
acrocephalosyndactylia
GENETIC ASSOCIATION
Gli3
NAMED AFTER
David Middleton Greig
Wikipedia
EN
Greig cephalopolysyndactyly syndrome
Wikidata
EN
Greig cephalopolysyndactyly syndrome
Wikipedia Redirections
EN
cephalopolysyndactyly syndrome, GCPS, Greig cephalopolysyndactyly, Greig cephalopolysyndactyly (GCPS) syndrome, Greig syndrome
Wikidata Alias
EN
GCPS, GREIG CEPHALOPOLYSYNDACTYLY SYNDROME, GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS, Greig Cephalosyndactyly Syndrome, Greig syndrome, Polysyndactyly With Peculiar Skull Shape, polysyndactyly with peculiars skull shape

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