serpin family E member 1
OMIM: 173360, Gene2Phenotype
| Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| SERPINE1 in Bleeding and Platelet Disorders
                    
                    
                       | 1 review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Sources
 Phenotypes
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| SERPINE1 in Mendeliome
                    
                    
                     | 1 review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Sources
 Phenotypes
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| SERPINE1 in Transplant Co-Morbidity
                    
                    
                       | 0 reviews | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Sources
 Phenotypes
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