Vertebral compression fractures

Symptom Information:

Symptom ID: HPO:0002953
Synonyms:
Fractures of vertebral bodies [HPO:0002953]
Vertebral body compression [HPO:0002953]
Vertebral collapse [HPO:0002953]
Vertebral compression [HPO:0002953]
Vertebral compression or collapse [HPO:0002953]
Fractures of vertebral bodies [OMIM:Fractures of vertebral bodies]
Vertebral collapse [OMIM:Vertebral collapse]
Vertebral compression [OMIM:Vertebral compression]
Vertebral compression fractures [OMIM:Vertebral compression fractures]
Vertebral compression or collapse [OMIM:Vertebral compression or collapse]
Vertebral compression fractures (8/8 patients) [OMIM:Vertebral compression fractures (8/8 patients)]
Quality:
Cross references:
OMIM: "Fractures of vertebral bodies" [OMIM:Fractures of vertebral bodies]
OMIM: "Vertebral collapse" [OMIM:Vertebral collapse]
OMIM: "Vertebral compression" [OMIM:Vertebral compression]
OMIM: "Vertebral compression fractures" [OMIM:Vertebral compression fractures]
OMIM: "Vertebral compression or collapse" [OMIM:Vertebral compression or collapse]
OMIM: "Vertebral compression fractures (8/8 patients)" [OMIM:Vertebral compression fractures (8/8 patients)]
Is a (Direct Parents):
HPO         Abnormality of the vertebrae
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the vertebrae(HPO:0003468)
                      Vertebral compression fractures(HPO:0002953)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Cole-Carpenter syndrome (Orphanet:2050)
Congenital erythropoietic porphyria (Orphanet:79277)
Cushing disease (Orphanet:96253)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Geroderma osteodysplastica (Orphanet:2078)
HAJDU-CHENEY SYNDROME (OMIM:102500)
OSTEOGENESIS IMPERFECTA, TYPE VI (OMIM:613982)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
OSTEOGENESIS IMPERFECTA, TYPE XI (OMIM:610968)
PAGET DISEASE OF BONE (OMIM:602080)
Spondylo-ocular syndrome (Orphanet:85194)
Torg-Winchester syndrome (Orphanet:3460)