Term info
- DOID:2219 (MONDO:equivalentTo)
- OMIM:273800 (Orphanet:849/e)
- MESH:D013915 (MONDO:equivalentTo)
- NCIT:C61249 (MONDO:equivalentTo)
- SCTID:32942005 (MONDO:equivalentTo)
- GARD:0002478 (MONDO:equivalentTo)
ordo_disease
A bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia
http://identifiers.org/snomedct/32942005, http://purl.obolibrary.org/obo/NCIT_C61249, http://identifiers.org/mesh/D013915, http://purl.obolibrary.org/obo/DOID_2219, https://omim.org/entry/273800
Glanzmann's thrombasthenia, Glanzmann thrombasthenia
platelet glycoprotein IIb-IIIa deficiency, glycoprotein IIb/IIIa defect, Glanzmann thrombasthenia 1, deficiency of GP IIb-IIIa complex, Thrombocytasthenia, deficiency of glycoprotein complex IIb-IIIa, platelet-type bleeding disorder 2, deficiency of platelet fibrinogen receptor, thrombasthenia, thrombasthenia of Glanzmann and Naegeli, BDPLT2
deficiency of GP 2B 3A complex, bleeding disorder, Platelet-type, 2, Diacyclothrombopathia 2B 3A, Platelet fibrinogen receptor, deficiency of, Platelet glycoprotein 2B 3A deficiency, GP IIb-IIIa Complex, deficiency of, Platelet glycoprotein IIb-IIIa deficiency, glycoprotein Complex IIb-IIIa, deficiency of, GT, Glanzmann thrombasthenia type A
MONDO:0031332