Gray Platelet Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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1 genes/proteins associated with the disease Gray Platelet Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NBEAL2 neurobeachin-like 2 2.88009