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bn:16842932n
Noun Concept
Categories: Autosomal recessive disorders, Diseases named for discoverer
EN
Baller-Gerold syndrome  Baller–Gerold syndrome  BALLER-GEROLD SYNDROME; BGS  BGS  Craniosynostosis-Radial Aplasia Syndrome
EN
Baller–Gerold syndrome is a rare genetic syndrome that involves premature fusion of the skull bones and malformations of facial, forearm and hand bones. Wikipedia
Definitions
Relations
Sources
EN
Baller–Gerold syndrome is a rare genetic syndrome that involves premature fusion of the skull bones and malformations of facial, forearm and hand bones. Wikipedia
Synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone Wikidata
A rare genetic disorder characterized by an abnormally shaped skull, short stature, and aplasia or hypoplasia of the radius bone in the forearm. Wiktionary
IS A
disease
rare disease
synostosis
GENETIC ASSOCIATION
RECQL4
Wikipedia
EN
Baller–Gerold syndrome
Wikidata
EN
Baller-Gerold syndrome
Wiktionary
EN
Baller-Gerold syndrome
Wikipedia Redirections
EN
Baller-Gerold syndrome
Wikidata Alias
EN
BALLER-GEROLD SYNDROME, BALLER-GEROLD SYNDROME; BGS, BGS, Craniosynostosis-Radial Aplasia Syndrome, Craniosynostosis With Radial Defects

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