Polysplenia
Symptom Information:
Symptom ID: | HPO:0001748 | ||||||||||||
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) Polysplenia(HPO:0001748) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the spleen(HPO:0001743) Supernumerary spleens(HPO:0009799) Polysplenia(HPO:0001748) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Spleen disorders(MedDRA:10041635) Polysplenia(HPO:0001748) |
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Database Frequency: | 14 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Acrocephalopolydactyly | (Orphanet:221054) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CILIARY DYSKINESIA, PRIMARY, 14 | (OMIM:613807) |
Campomelia, Cumming type | (Orphanet:1318) |
Carpenter syndrome | (Orphanet:65759) |
Feingold syndrome | (Orphanet:1305) |
Fryns syndrome | (Orphanet:2059) |
HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Ivemark syndrome | (Orphanet:97548) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |