Details of Disease

General Information of Disease (ID: DIST7129)

Disease Name Thrombophilia, familial, due to decreased release of tissue plasminogen activator
Synonyms
hyperfibrinolysis, familial, due to increased release of tissue plasminogen activator; hyperfibrinolysis, familial, due to increased release of plat; thrombophilia, familial, due to decreased release of PLAT; thrombophilia, familial, due to decreased release of tissue plasminogen activator; THPH9
Disease Hierarchy
DISFG8KS: Inherited thrombophilia
DIST7129: Thrombophilia, familial, due to decreased release of tissue plasminogen activator
Disease Identifiers
MONDO ID
MONDO_0012872
MESH ID
C567341
UMLS CUI
C2676721
OMIM ID
612348
MedGen ID
393574

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
PLAT TTXAGYU Moderate 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
PLAT OTQPDNAB Moderate Autosomal recessive [1]
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References

1 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.