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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 17/07/2006 |
| Symbol | KNG |
| Location | 3q27.3 |
| Name | kininogen deficiency |
| Other name(s) |
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| Corresponding gene | KNG1 |
| Main clinical features | deficiency of a procoagulant Flaujeac factor, which, like Hageman and Fletcher factors, participates in the 'contact phase' of coagulation, asymptomatic |
| Genetic determination | autosomal recessive |
| Function/system disorder | hematology |
| Type | disease |
| Gene product |
| Name | kininogen, high molecular weight (KNG) |
| Remark(s) |