Accessory spleen
Symptom Information:
Symptom ID: | HPO:0001747 | ||||||||
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 immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the spleen(HPO:0001743) Supernumerary spleens(HPO:0009799) Accessory spleen(HPO:0001747) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) Supernumerary spleens(HPO:0009799) Accessory spleen(HPO:0001747) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Accessory spleen(HPO:0001747) |
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Database Frequency: | 8 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Feingold syndrome | (Orphanet:1305) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Hydrolethalus | (Orphanet:2189) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
ROBERTS SYNDROME | (OMIM:268300) |
Roberts syndrome | (Orphanet:3103) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |