Polysplenia

Symptom Information:

Symptom ID: HPO:0001748
Synonyms:
Accessory spleens [HPO:0001748]
Multiple accessory spleens [HPO:0001748]
Accessory spleen [Orphanet:31300]
Accessory spleen (disorder) [Orphanet:31300]
Accessory spleens [OMIM:Accessory spleens]
Multiple accessory spleens [OMIM:Multiple accessory spleens]
Polysplenia [OMIM:Polysplenia]
Asplenia/polysplenia/spleen lobulation/accessory spleen [Orphanet:31300]
Accessory spleen [MedDRA:10068059]
Spleen lobulation [Orphanet:31300]
Congenital lobulation of spleen (disorder) [Orphanet:31300]
Congenital lobulation of spleen [Orphanet:31300]
Quality:
Cross references:
HPO:0001747 "Accessory spleen" [Orphanet:31300]
Orphanet:31300 "Asplenia/polysplenia/spleen lobulation/accessory spleen" [Orphanet:31300]
OMIM: "Accessory spleens" [OMIM:Accessory spleens]
OMIM: "Multiple accessory spleens" [OMIM:Multiple accessory spleens]
OMIM: "Polysplenia" [OMIM:Polysplenia]
UMLS:C0266631 "Accessory spleen" [Orphanet:31300]
UMLS:C0266635 "Congenital lobulation of spleen" [Orphanet:31300]
Is a (Direct Parents):
Orphanet Abnormality of the spleen
MedDRA Spleen disorders
HPO         Supernumerary spleens
Orphanet Asplenia
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)
                Supernumerary spleens(HPO:0009799)
                   Polysplenia(HPO:0001748)
       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)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Spleen disorders(MedDRA:10041635)
          Polysplenia(HPO:0001748)
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)