|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Gray platelet syndrome (GPS) is a rare inherited bleeding disorder characterized by macrothrombocytopenia, myelofibrosis, splenomegaly and typical gray appearance of platelets on Wright stained peripheral blood smear. (Orphanet Rare Disease Ontology, Orphanet_721)|
|Downloads & Tools|
1 genes/proteins associated with the disease Gray Platelet Syndrome from the curated CTD Gene-Disease Associations dataset.