coagulation factor XI
OMIM: 264900, Gene2Phenotype
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F11 in Bleeding and Platelet Disorders
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
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Phenotypes
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F11 in Mendeliome
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
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Phenotypes
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F11 in Additional findings_Paediatric
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review | BIALLELIC, autosomal or pseudoautosomal |
Sources
Phenotypes
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F11 in Prepair 1000+
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
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Phenotypes
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F11 in BabyScreen+ newborn screening
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
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Phenotypes
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F11 in Transplant Co-Morbidity Superpanel
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
Sources
Phenotypes
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