fibrinogen gamma chain
OMIM: 134850, Gene2Phenotype
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FGG in Inherited bleeding disorders
Level 3: Haemostasis 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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FGG in Thrombophilia with a likely monogenic cause
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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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FGG 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 |
Sources
Phenotypes
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FGG in Severe Paediatric Disorders
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
Sources
Phenotypes
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