Warfarin-induced skin necrosis
Symptom Information:
Symptom ID: | HPO:0001038 | ||
Synonyms: |
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Quality: | |||
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 the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Dermatological manifestations of systemic disorders(HPO:0001005) Warfarin-induced skin necrosis(HPO:0001038) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Protein S acquired deficiency | (Orphanet:26349) |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT | (OMIM:176860) |