Dysfibrinogenemia
(Q5319404)
Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen
Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen
Language:
Current Data About
Dysfibrinogenemia
| (P31) |
(Q112193867)
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| (P279) |
(Q42416071)
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| (P1692) |
286.3
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| (P1748) |
C131659
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| (P2293) |
(Q17928227)
(Q5446444)
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| (P2888) |
http://www.orpha.net/ORDO/Orphanet_248408
http://www.orpha.net/ORDO/Orphanet_335 http://www.orpha.net/ORDO/Orphanet_98881 |
other details
| aliases |
Congenital dysfibrinogenemia Familial dysfibrinogenemia DYSFIBRINOGENEMIA, CONGENITAL Dysfibrinogenemia, familial Hypodysfibrinogenemia, Congenital |
| description | Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen |
External Links
| (P492) |
616004
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| (P1550) |
98881
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| (P2892) |
C1260903
C0272350 C5681639 |
| (P4229) |
D68.2
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| (P4233) |
dysfibrinogenemia
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| (P4317) |
2004
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| (P5270) |
MONDO_0014452
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| (P6366) |
2777902675
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| (P7807) |
815934276
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| (P11430) |
DI-04218
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