Hyperfibrinogenemia
Symptom Information:
| Symptom ID: | HPO:0011899 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of coagulation(HPO:0001928) Abnormality of the coagulation cascade(HPO:0003256) Abnormality of the common coagulation pathway(HPO:0010990) Abnormality of circulating fibrinogen(HPO:0011898) Hyperfibrinogenemia(HPO:0011899) MedDRA: |
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| Database Frequency: | 1 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Neonatal hemochromatosis | (Orphanet:446) |