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Glanzmann thrombasthenia 1

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia

Synonyms

  • BDPLT2
  • Diacyclothrombopathia 2B 3A
  • GP IIb-IIIa Complex, deficiency of
  • GT
  • Glanzmann thrombasthenia
  • Glanzmann thrombasthenia 1
  • Glanzmann thrombasthenia type A
  • Glanzmann's thrombasthenia
  • Platelet fibrinogen receptor, deficiency of
  • Platelet glycoprotein 2B 3A deficiency
  • Platelet glycoprotein IIb-IIIa deficiency
  • Thrombocytasthenia
  • bleeding disorder, Platelet-type, 2
  • deficiency of GP 2B 3A complex
  • deficiency of GP IIb-IIIa complex
  • deficiency of glycoprotein complex IIb-IIIa
  • deficiency of platelet fibrinogen receptor
  • glycoprotein Complex IIb-IIIa, deficiency of
  • glycoprotein IIb/IIIa defect
  • platelet glycoprotein IIb-IIIa deficiency
  • platelet-type bleeding disorder 2
  • thrombasthenia
  • thrombasthenia of Glanzmann and Naegeli
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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MedlinePlus

MedlinePlus has information about this condition that may include a description, frequency, causes, inheritance, and links to more information. The information is written for the public, including patients, caregivers and families. MedlinePlus is a service of the National Library of Medicine (NLM), which is part of the National Institutes of Health (NIH).

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