Holt-Oram syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Holt-Oram syndrome (HOS) is the most common form of heart-hand syndrome (see this term) and is characterized by skeletal abnormalities of the upper limbs and mild-to-severe congenital cardiac defects. (Orphanet Rare Disease Ontology, Orphanet_392)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535326
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Genes

1 genes/proteins associated with the disease Holt-Oram syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TBX5 T-box 5 2.88009