Orphanet: Baller Gerold syndrome

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Baller-Gerold syndrome

Disease definition

Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).


Classification level: Disorder
  • Synonym(s): -
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Neonatal
  • ICD-10: Q75.0
  • OMIM: 218600
  • UMLS: C0265308
  • MeSH: C536788
  • GARD: 1602
  • MedDRA: -

Detailed information


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