Congenital Plasminogen Activator Inhibitor Type 1 Deficiency
| Disease Aliases (8) | Congenital pai-1 deficiency Hyperfibrinolysis due to pai1 deficiency Pai-1 deficiency Pai1 deficiency Plasminogen activator inhibitor 1 deficiency Congenital plasminogen activator inhibitor type 1 deficiency Plasminogen activator inhibitor-1 deficiency |
Associated Genes (1) NCBI-RefSeq: SERPINE1 (Serpin family E member 1) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Congenital plasminogen activator inhibitor type 1 deficiency | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |