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| Congenital afibrinogenemia Classification and external resources |
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| ICD-10 | D65. |
|---|---|
| ICD-9 | 286.3 |
| OMIM | 202400 |
| DiseasesDB | 307 |
| MedlinePlus | 001313 |
| eMedicine | ped/3042 |
| MeSH | D000347 |
Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation. [1]
References
- ^ Neerman-Arbez M, de Moerloose P (2007). "Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations". Hum. Mutat. 28 (6): 540–53. doi:. PMID 17295221.
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- This page was last modified on 28 May 2008, at 13:04.
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