Reduced antithrombin III activity
Symptom Information:
Symptom ID: | HPO:0001976 | ||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Reduced antithrombin III activity(HPO:0001976) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Coagulation factor deficiencies(MedDRA:10009737) Reduced antithrombin III activity(HPO:0001976) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Coagulation and bleeding analyses(MedDRA:10009728) Reduced antithrombin III activity(HPO:0001976) |
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Database Frequency: | 10 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
ALG6-CDG | (Orphanet:79320) |
DK1-CDG | (Orphanet:91131) |
DPAGT1-CDG | (Orphanet:86309) |
DPM1-CDG | (Orphanet:79322) |
Hereditary thrombophilia due to congenital antithrombin deficiency | (Orphanet:82) |
MGAT2-CDG | (Orphanet:79329) |
MPI-CDG | (Orphanet:79319) |
PGM1-CDG | (Orphanet:319646) |
PMM2-CDG | (Orphanet:79318) |
SRD5A3-CDG | (Orphanet:324737) |