Preferred Name

gray platelet syndrome

Synonyms

platelet alpha-granule deficiency

Alpha storage pool deficiency

grey platelet syndrome

BDPLT4

platelet-type bleeding disorder 4

GPS

gray platelet syndrome

marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins

bleeding disorder, Platelet-type, 4

Definitions

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.

ID

http://purl.obolibrary.org/obo/MONDO_0007686

has_exact_synonym

platelet alpha-granule deficiency

Alpha storage pool deficiency

grey platelet syndrome

BDPLT4

platelet-type bleeding disorder 4

GPS

gray platelet syndrome

has_related_synonym

marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins

bleeding disorder, Platelet-type, 4

label

gray platelet syndrome

prefixIRI

MONDO:0007686

prefLabel

gray platelet syndrome

seeAlso

https://rarediseases.info.nih.gov/diseases/2562/gray-platelet-syndrome

textual definition

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.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0020117

http://purl.obolibrary.org/obo/MONDO_0000009

http://purl.obolibrary.org/obo/MONDO_0002254

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0007686 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007686 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007686 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_0111044 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0007686 EFO LOOM
http://purl.obolibrary.org/obo/DOID_0111044 DOID LOOM
http://purl.bioontology.org/ontology/MESH/D055652 MESH LOOM
http://purl.bioontology.org/ontology/OMIM/139090 OMIM LOOM
http://purl.jp/bio/4/id/200906048170483854 IOBC LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0272302 OCHV LOOM
http://identifiers.org/omim/139090 REXO LOOM
http://identifiers.org/omim/139090 GEXO LOOM
http://identifiers.org/omim/139090 RETO LOOM
http://purl.obolibrary.org/obo/OMIM_139090 CCO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D055652 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00037342 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/SNMI/DC-61940 SNMI LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.099.417 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0026406 OMIT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Gray_Platelet_Syndrome CSEO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84741 NCIT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_8697 HRDO LOOM
http://www.limics.fr/ontologies/ontolurgences#ThrombopathieDesPlaquettesGrises ONTOLURGENCES LOOM
http://purl.obolibrary.org/obo/NCIT_C84741 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.140.427 RH-MESH LOOM
http://www.orpha.net/ORDO/Orphanet_721 ORDO LOOM
http://purl.obolibrary.org/obo/DOID_0111044 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0111044 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0111044 FNS-H LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/51720005 SNOMEDCT LOOM