Splenic rupture
Symptom Information:
Symptom ID: | HPO:0012223 | ||||
Synonyms: |
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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 immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the spleen(HPO:0001743) Splenic rupture(HPO:0012223) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) Splenic rupture(HPO:0012223) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Splenic rupture(HPO:0012223) |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Congenital fibrinogen deficiency | (Orphanet:335) |
Familial afibrinogenemia | (Orphanet:98880) |
Familial dysfibrinogenemia | (Orphanet:98881) |
Familial hypodysfibrinogenemia | (Orphanet:248408) |
Familial hypofibrinogenemia | (Orphanet:101041) |
Marfan syndrome type 2 | (Orphanet:284973) |