Rubinstein-Taybi syndrome

Summary
Synonym
  • Broad Thumb-Hallux syndrome
  • Rubinstein syndrome
  • proximal chromosome 16p13.3 deletion syndrome
Definition
A syndrome characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes.
Super Class
autosomal dominant disease chromosomal deletion syndrome syndrome
Disease Ontology
DOID:1933
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1387 CREBBP CREB binding protein
2033 EP300 E1A binding protein p300
Displaying 1 entry
Gene ID Gene Symbol Description Source
328572 Ep300 E1A binding protein p300

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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