Details of Disease | DrugMAP

General Information of Disease (ID: DISWQ7BR)

Disease Name	Symptomatic form of hemophilia A in female carriers
Definition	A form of hemophilia A that manifests in some women with mutations in the F8 gene (Xq28), encoding coagulation factor VIII.
Disease Hierarchy	DIS0RQ2E: Haemophilia A DISWQ7BR: Symptomatic form of hemophilia A in female carriers
Disease Identifiers	MONDO ID MONDO_0015787 UMLS CUI C5680504 MedGen ID 1843218 Orphanet ID 177926

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
F8	TT1290U	Supportive	X-linked	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
F8	OTH6XHDU	Supportive	X-linked	[1]
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References

1	Hemophilia A. 2000 Sep 21 [updated 2023 Jul 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(?) [Internet]. Seattle (WA): University of Washington, Seattle; 1993C2024.