Accessory spleen

Symptom Information:

Symptom ID: HPO:0001747
Synonyms:
Accessory spleen (disorder) [Orphanet:31300]
Accessory spleen [Orphanet:31300]
Accessory spleen [OMIM:Accessory spleen]
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:0001748 "Polysplenia" [Orphanet:31300]
Orphanet:31300 "Asplenia/polysplenia/spleen lobulation/accessory spleen" [Orphanet:31300]
OMIM: "Accessory spleen" [OMIM:Accessory spleen]
UMLS:C0266631 "Accessory spleen" [Orphanet:31300]
UMLS:C0266635 "Congenital lobulation of spleen" [Orphanet:31300]
Is a (Direct Parents):
Orphanet Asplenia
HPO         Supernumerary spleens
MedDRA Spleen disorders
Orphanet Abnormality of the spleen
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)
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)