| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Reduction in the amount of kininogen, which functions as a cofactor in the contact phase of the intrinsic blood coagulation cascade. (Human Phenotype Ontology, HP_0005527) |
| External Link | http://www.omim.org/entry/228960 |
| Similar Terms | |
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1 genes associated with the [kininogen deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KNG1 | kininogen 1 |
