coagulation factor IX
OMIM: 300746, Gene2Phenotype
Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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F9 in Gene therapy clinical trials
Level 3: Clinical trials
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review | Not set |
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Phenotypes
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F9 in Inherited bleeding disorders
Level 3: Haemostasis disorders
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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F9 in Bleeding and platelet disorders
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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F9 in Severe Paediatric Disorders
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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F9 in Factor IX deficiency
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
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