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Rubinstein-Taybi syndrome due to CREBBP mutations

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any Rubinstein-Taybi syndrome in which the cause of the disease is a mutation in the CREBBP gene.
Uniprot Description A disorder characterized by craniofacial abnormalities, postnatal growth deficiency, broad thumbs, broad big toes, mental retardation and a propensity for development of malignancies.
Mondo Term and Equivalent IDs
MONDO:0008393:  Rubinstein-Taybi syndrome due to CREBBP mutations
NCIT:C153290: 
Orphanet:353277: