Hypersplenism

Symptom Information:

Symptom ID: HPO:0001971
Synonyms:
Hypersplenism (disorder) [Orphanet:31900]
Hypersplenism [Orphanet:31900]
Hypersplenism [OMIM:Hypersplenism]
Hypersplenism [MedDRA:10020769]
Hypersplenism acquired [MedDRA:10020769]
Splenic sequestration [MedDRA:10020769]
Splenic sequestration crisis [MedDRA:10020769]
Quality:
Cross references:
Orphanet:31900 "Hypersplenism" [Orphanet:31900]
OMIM: "Hypersplenism" [OMIM:Hypersplenism]
UMLS:C0020532 "Hypersplenism" [HPO:0001971]
UMLS:C0020532 "Hypersplenism" [Orphanet:31900]
Is a (Direct Parents):
Orphanet Abnormality of the spleen
HPO         Abnormality of the spleen
MedDRA Spleen disorders
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)
                Hypersplenism(HPO:0001971)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the spleen(HPO:0001743)
                Hypersplenism(HPO:0001971)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Spleen disorders(MedDRA:10041635)
          Hypersplenism(HPO:0001971)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
Alpha-thalassemia (Orphanet:846)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Beta-thalassemia associated with another hemoglobin anomaly (Orphanet:231230)
Beta-thalassemia major (Orphanet:231214)
Gaucher disease type 1 (Orphanet:77259)
SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T HELPER CELLS (OMIM:183350)
Wilson disease (Orphanet:905)