loading...| Preferred Name | Glanzmann Thrombasthenia | |
| Synonyms |
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| Definitions |
A rare, autosomal recessive inherited and less frequently acquired platelet disorder. It is characterized by deficient or dysfunctional glycoprotein IIb/IIIa complex. It leads to defective platelet aggregation, resulting in bleeding. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C61249 |
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| ALT_DEFINITION |
A rare, autosomal recessive inherited, and less frequently acquired, platelet disorder that is characterized by deficient or dysfunctional glycoprotein IIb/IIIa complex, which leads to defective platelet aggregation, resulting in bleeding. |
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| code |
C61249 |
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| Contributing_Source |
NICHD |
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| definition |
A rare, autosomal recessive inherited and less frequently acquired platelet disorder. It is characterized by deficient or dysfunctional glycoprotein IIb/IIIa complex. It leads to defective platelet aggregation, resulting in bleeding. |
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| in_subset | ||
| label |
Glanzmann Thrombasthenia |
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| Legacy Concept Name |
Glanzmann_Thrombasthenia |
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| Preferred_Name |
Glanzmann Thrombasthenia |
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| prefixIRI |
NCIT:C61249 |
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| prefLabel |
Glanzmann Thrombasthenia |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0040015 |
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| subClassOf |