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GENATLAS PHENOTYPE |
last update : 04-04-2013 |
Symbol | F10D |
Location | 13q34 |
Name | factor X deficiency |
Other name(s) | Stuart-Power factor deficiency |
Corresponding gene | F10 |
Main clinical features | bleeding diathesis, bleeding disorder caused by diverse mutations |
Genetic determination | autosomal recessive |
Function/system disorder | hematology |
Type | disease |
Gene product |
Name | coagulation factor X (F10) |
Remark(s) |
Genotype/Phenotype correlations |
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