|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Holt-Oram syndrome from the curated CTD Gene-Disease Associations dataset.