Hypersplenism
Symptom Information:
Symptom ID: | HPO:0001971 | |||||||
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 the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) Hypersplenism(HPO:0001971) Abnormality of the immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the spleen(HPO:0001743) Hypersplenism(HPO:0001971) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Hypersplenism(HPO:0001971) |
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Database Frequency: | 8 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
Alpha-thalassemia | (Orphanet:846) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Beta-thalassemia associated with another hemoglobin anomaly | (Orphanet:231230) |
Beta-thalassemia major | (Orphanet:231214) |
Gaucher disease type 1 | (Orphanet:77259) |
SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T HELPER CELLS | (OMIM:183350) |
Wilson disease | (Orphanet:905) |