Plasminogen Activator Inhibitor-1 Deficiency (PAI-1D)

Alias:
Congenital Plasminogen Activator Inhibitor Type 1 Deficiency
Deficiency, Plasminogen Activator Inhibitor-1
Hyperfibrinolysis Due to Pai1 Deficiency
Plasminogen Activator Inhibitor, Type I
Pai-1d
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Plasminogen Activator Inhibitor-1 Deficiency, also known as congenital plasminogen activator inhibitor type 1 deficiency, is related to complete plasminogen activator inhibitor 1 deficiency and congenital plasminogen activator inhibitor type 1 deficiency. An important gene associated with Plasminogen Activator Inhibitor-1 Deficiency is SERPINE1 (Serpin Family E Member 1). The drugs Metformin and Plasminogen Activator Inhibitor 1 have been mentioned in the context of this disorder. Affiliated tissues include smooth muscle and endothelial, and related phenotypes are abnormal bleeding and menorrhagia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
7
7

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
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Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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