Reduced antithrombin III activity

Symptom Information:

Symptom ID: HPO:0001976
Synonyms:
Anti-thrombin III deficiency [HPO:0001976]
Antithrombin III deficiency [HPO:0001976]
Decreased antithrombin III [HPO:0001976]
Anti-thrombin III deficiency [OMIM:Anti-thrombin III deficiency]
Antithrombin III deficiency [OMIM:Antithrombin III deficiency]
Decreased antithrombin III [OMIM:Decreased antithrombin III]
Antithrombin III deficiency (in 1 patient) [OMIM:Antithrombin III deficiency (in 1 patient)]
Decreased antithrombin III (1 patient) [OMIM:Decreased antithrombin III (1 patient)]
Antithrombin III deficiency [MedDRA:10002832]
Antithrombin III decreased [MedDRA:10049547]
Quality:
Cross references:
OMIM: "Anti-thrombin III deficiency" [OMIM:Anti-thrombin III deficiency]
OMIM: "Antithrombin III deficiency" [OMIM:Antithrombin III deficiency]
OMIM: "Decreased antithrombin III" [OMIM:Decreased antithrombin III]
OMIM: "Antithrombin III deficiency (in 1 patient)" [OMIM:Antithrombin III deficiency (in 1 patient)]
OMIM: "Decreased antithrombin III (1 patient)" [OMIM:Decreased antithrombin III (1 patient)]
Is a (Direct Parents):
MedDRA Coagulation and bleeding analyses
MedDRA Coagulation factor deficiencies
HPO         Abnormality of the coagulation cascade
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:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          Reduced antithrombin III activity(HPO:0001976)
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)
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)