loading...| Preferred Name | Glanzmann thrombasthenia | |
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| Definitions |
(GT): A common inherited disease of platelet aggregation. It is characterized by mucocutaneous bleeding of mild-to-moderate severity. GT has been classified clinically into types I and II. In type I, platelets show absence of the glycoprotein IIb-IIIa complexes at their surface and lack fibrinogen and clot retraction capability. In type II, the platelets express the GPIIb-IIIa complex at reduced levels, have detectable amounts of fibrinogen, and have low or moderate clot retraction capability. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_273800 |
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| definition |
(GT): A common inherited disease of platelet aggregation. It is characterized by mucocutaneous bleeding of mild-to-moderate severity. GT has been classified clinically into types I and II. In type I, platelets show absence of the glycoprotein IIb-IIIa complexes at their surface and lack fibrinogen and clot retraction capability. In type II, the platelets express the GPIIb-IIIa complex at reduced levels, have detectable amounts of fibrinogen, and have low or moderate clot retraction capability. |
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| has_obo_namespace |
cell_cycle_ontology |
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| id |
OMIM:273800 |
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| label |
Glanzmann thrombasthenia |
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| notation |
OMIM:273800 |
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| prefLabel |
Glanzmann thrombasthenia |
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