Abnormality of the intrinsic pathway
Symptom Information:
Symptom ID: | HPO:0010989 | ||
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Is a (Whole tree): |
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 intrinsic pathway(HPO:0010989) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT | (OMIM:300807) |