Cerebellar hemorrhage

Symptom Information:

Symptom ID: HPO:0011695
Synonyms:
Cerebellar hemorrhage (rare) [OMIM:Cerebellar hemorrhage (rare)]
Quality:
Cross references:
OMIM: "Cerebellar hemorrhage (rare)" [OMIM:Cerebellar hemorrhage (rare)]
Is a (Direct Parents):
HPO         Intracranial hemorrhage
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Abnormality of blood circulation(HPO:0011028)
                Internal hemorrhage(HPO:0011029)
                   Intracranial hemorrhage(HPO:0002170)
                      Cerebellar hemorrhage(HPO:0011695)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the cerebral vasculature(HPO:0100659)
                Intracranial hemorrhage(HPO:0002170)
                   Cerebellar hemorrhage(HPO:0011695)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Intracranial hemorrhage(HPO:0002170)
                   Cerebellar hemorrhage(HPO:0011695)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Isovaleric acidemia (Orphanet:33)
Propionic acidemia (Orphanet:35)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)