Arterial thrombosis

Symptom Information:

Symptom ID: HPO:0004420
Synonyms:
Arterial thrombosis (disorder) [Orphanet:35300]
Arterial thrombosis [Orphanet:35300]
Arterial thrombosis [OMIM:Arterial thrombosis]
Arterial embolism/thrombosis [Orphanet:35300]
Arterial thrombosis [MedDRA:10003178]
Arterial thrombosis NOS [MedDRA:10003178]
Thrombosis arterial [MedDRA:10003178]
Atherothrombosis [MedDRA:10003178]
Embolism arterial [MedDRA:10014513]
Arterial embolism [Orphanet:35300]
Arterial embolism (disorder) [Orphanet:35300]
Quality:
Cross references:
Orphanet:35300 "Arterial embolism/thrombosis" [Orphanet:35300]
OMIM: "Arterial thrombosis" [OMIM:Arterial thrombosis]
UMLS:C0151942 "Arterial thrombosis" [Orphanet:35300]
UMLS:C0549124 "Arterial embolism" [Orphanet:35300]
Is a (Direct Parents):
HPO         Abnormal thrombosis
Orphanet Abnormality of cardiovascular system physiology
MedDRA Non-site specific embolism and thrombosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal thrombosis(HPO:0001977)
             Arterial thrombosis(HPO:0004420)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Thromboembolism(HPO:0001907)
       Non-site specific embolism and thrombosis(MedDRA:10014524)
          Arterial thrombosis(HPO:0004420)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

ANTIPHOSPHOLIPID SYNDROME, FAMILIAL (OMIM:107320)
Behçet disease (Orphanet:117)
Buerger disease (Orphanet:36258)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Classical homocystinuria (Orphanet:394)
Cogan syndrome (Orphanet:1467)
Ebstein malformation (Orphanet:1880)
Essential thrombocythemia (Orphanet:3318)
Familial thrombocytosis (Orphanet:71493)
Giant cell arteritis (Orphanet:397)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hughes-Stovin syndrome (Orphanet:228116)
Malignant atrophic papulosis (Orphanet:679)
Polyarteritis nodosa (Orphanet:767)
Polycythemia vera (Orphanet:729)
Protein S acquired deficiency (Orphanet:26349)
Proteus syndrome (Orphanet:744)
Relapsing polychondritis (Orphanet:728)
Secondary polycythemia (Orphanet:98428)
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:614514)