Asplenia

Symptom Information:

Symptom ID: HPO:0001746
Synonyms:
Spleen absent (finding) [Orphanet:31300]
Congenital absence of spleen (disorder) [Orphanet:31300]
Spleen absent [Orphanet:31300]
Congenital absence of spleen [Orphanet:31300]
Asplenia [OMIM:Asplenia]
Asplenia/polysplenia/spleen lobulation/accessory spleen [Orphanet:31300]
Asplenia [Orphanet:31300]
Asplenia [MedDRA:10053622]
Asplenia (in some patients) [OMIM:Asplenia (in some patients)]
Asplenia (rare) [OMIM:Asplenia (rare)]
Spleen lobulation [Orphanet:31300]
Congenital lobulation of spleen (disorder) [Orphanet:31300]
Congenital lobulation of spleen [Orphanet:31300]
Quality:
Cross references:
Orphanet:31300 "Asplenia/polysplenia/spleen lobulation/accessory spleen" [Orphanet:31300]
OMIM: "Asplenia" [OMIM:Asplenia]
OMIM: "Asplenia (in some patients)" [OMIM:Asplenia (in some patients)]
OMIM: "Asplenia (rare)" [OMIM:Asplenia (rare)]
UMLS:C0600031 "Asplenia" [HPO:0001746]
UMLS:C0577288 "Spleen absent" [Orphanet:31300]
UMLS:C0600031 "Congenital absence of spleen" [Orphanet:31300]
UMLS:C0266635 "Congenital lobulation of spleen" [Orphanet:31300]
Is a (Direct Parents):
MedDRA Spleen disorders
Orphanet Abnormality of the spleen
HPO         Aplasia/Hypoplasia of the spleen
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)
                Aplasia/Hypoplasia of the spleen(HPO:0010451)
                   Asplenia(HPO:0001746)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of the lymphatic system(HPO:0100763)
             Abnormality of the spleen(HPO:0001743)
                Aplasia/Hypoplasia of the spleen(HPO:0010451)
                   Asplenia(HPO:0001746)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Spleen disorders(MedDRA:10041635)
          Asplenia(HPO:0001746)
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
Familial isolated congenital asplenia (Orphanet:101351)
Feingold syndrome (Orphanet:1305)
HETEROTAXY, VISCERAL, 1, X-LINKED (OMIM:306955)
Isolated congenital hypoglossia/aglossia (Orphanet:141152)
Ivemark syndrome (Orphanet:97548)
LATERALITY DEFECTS, AUTOSOMAL DOMINANT (OMIM:601086)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Microgastria - limb reduction defect (Orphanet:2538)
Mowat-Wilson syndrome (Orphanet:2152)
Osteocraniostenosis (Orphanet:2763)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 (OMIM:615415)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
Tetraamelia - multiple malformations (Orphanet:3301)