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Disease Ontology Browser
Rubinstein-Taybi syndrome (DOID:1933)
Alliance: disease page
Synonyms: Broad Thumb-Hallux syndrome; proximal chromosome 16p13.3 deletion syndrome; Rubinstein syndrome
Alt IDs: OMIM:180849, OMIM:610543, OMIM:613684, ICD10CM:Q87.2, MESH:D012415, NCI:C75466, ORDO:783, UMLS_CUI:C0035934
Definition: A syndrome characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/27/2022
MGI 6.21
The Jackson Laboratory