Blood completely incoagulable
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 5 / 7739 | |
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All diseases associated with this symptom:
| Congenital fibrinogen deficiency | (Orphanet:335) |
| Familial afibrinogenemia | (Orphanet:98880) |
| Familial dysfibrinogenemia | (Orphanet:98881) |
| Familial hypodysfibrinogenemia | (Orphanet:248408) |
| Familial hypofibrinogenemia | (Orphanet:101041) |