Arterial thrombosis
Symptom Information:
Symptom ID: | HPO:0004420 | |||||||||||
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) 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) |
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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) |