Splenic rupture

Symptom Information:

Symptom ID: HPO:0012223
Synonyms:
Ruptured spleen [HPO:0012223]
Splenic rupture [OMIM:Splenic rupture]
Splenic rupture [MedDRA:10041658]
Quality:
Cross references:
OMIM: "Splenic rupture" [OMIM:Splenic rupture]
Is a (Direct Parents):
HPO         Abnormality of the spleen
MedDRA Spleen disorders
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)
                Splenic rupture(HPO:0012223)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of the lymphatic system(HPO:0100763)
             Abnormality of the spleen(HPO:0001743)
                Splenic rupture(HPO:0012223)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Spleen disorders(MedDRA:10041635)
          Splenic rupture(HPO:0012223)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Congenital fibrinogen deficiency (Orphanet:335)
Familial afibrinogenemia (Orphanet:98880)
Familial dysfibrinogenemia (Orphanet:98881)
Familial hypodysfibrinogenemia (Orphanet:248408)
Familial hypofibrinogenemia (Orphanet:101041)
Marfan syndrome type 2 (Orphanet:284973)