Details of Disease | DrugMAP

General Information of Disease (ID: DISR66KM)

Disease Name	Glanzmann thrombasthenia 2
Synonyms	GT2; Glanzmann thrombasthenia 2; bleeding disorder, platelet-type, 23
Disease Hierarchy	DISFGGTG: Glanzmann thrombasthenia DISR66KM: Glanzmann thrombasthenia 2
Disease Identifiers	MONDO ID MONDO_0031009 UMLS CUI C5543273 OMIM ID 619267 MedGen ID 1782592

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
ITGB3	TTJA1ZO	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ITGB3	OTWCK1K6	Strong	Autosomal recessive	[1]
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References

1	Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models. Blood. 2011 Dec 1;118(23):5996-6005. doi: 10.1182/blood-2011-07-365635. Epub 2011 Sep 13.