Details of Disease | DrugMAP

General Information of Disease (ID: DIS6JB6I)

Disease Name	Bleeding disorder, platelet-type, 22
Synonyms	BDPLT22; BLEEDING DISORDER, PLATELET-TYPE, 22
Disease Hierarchy	DISIUNXT: Inherited bleeding disorder, platelet-type DIS6JB6I: Bleeding disorder, platelet-type, 22
Disease Identifiers	MONDO ID MONDO_0032765 UMLS CUI C5193111 OMIM ID 618462 MedGen ID 1673822

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
EPHB2	TTKPV6O	Limited	Unknown	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
EPHB2	OT8VZ6C5	Limited	Unknown	[1]
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References

1	Towards the identification of a genetic basis for Landau-Kleffner syndrome. Epilepsia. 2014 Jun;55(6):858-65. doi: 10.1111/epi.12645. Epub 2014 May 14.