Gray platelet syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/139090
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Genes

1 genes associated with the Gray platelet syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
NBEAL2 neurobeachin-like 2