cerebrocostomandibular syndrome

Summary
Synonym
  • CCM syndrome
  • CCMS
  • cerebro-costo-mandibular syndrome
  • rib gap defects with micrognathia
Definition
A syndrome characterized by severe micrognathia, posterior rib and palate defects, and often intellectual disability that has_material_basis_in heterozygous mutation in SNRPB on 20p13.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0111248
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6628 SNRPB small nuclear ribonucleoprotein polypeptides B and B1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024