WormBase Tree Display for DO_term: DOID:2236
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| DOID:2236 | Name | congenital afibrinogenemia | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I). | ||||
| Comment | OMIM mapping confirmed by DO. | ||||
| Synonym | Exact | Factor I deficiency | |||
| Fibrinogen deficiency | |||||
| Parent | Is_a | DOID:1247 | |||
| DOID:0080015 | |||||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 202400 | |
| Attribute_of | Gene_by_orthology | WBGene00012782 |
