Thoracic kyphosis

Symptom Information:

Symptom ID: HPO:0002942
Synonyms:
Accentuated thoracic kyphosis [HPO:0002942]
Exaggerated thoracic kyphosis [HPO:0002942]
Accentuated thoracic kyphosis [OMIM:Accentuated thoracic kyphosis]
Exaggerated thoracic kyphosis [OMIM:Exaggerated thoracic kyphosis]
Thoracic kyphosis [OMIM:Thoracic kyphosis]
Quality:
Cross references:
OMIM: "Accentuated thoracic kyphosis" [OMIM:Accentuated thoracic kyphosis]
OMIM: "Exaggerated thoracic kyphosis" [OMIM:Exaggerated thoracic kyphosis]
OMIM: "Thoracic kyphosis" [OMIM:Thoracic kyphosis]
Is a (Direct Parents):
HPO         Kyphosis
HPO         Abnormality of the thoracic spine
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 thorax(HPO:0000765)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic kyphosis(HPO:0002942)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic kyphosis(HPO:0002942)
                   Abnormality of the curvature of the vertebral column(HPO:0010674)
                      Kyphosis(HPO:0002808)
                         Thoracic kyphosis(HPO:0002942)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
Czech dysplasia, metatarsal type (Orphanet:137678)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Gaucher disease type 3 (Orphanet:77261)
KAHRIZI SYNDROME (OMIM:612713)
KBG syndrome (Orphanet:2332)
Leber plus disease (Orphanet:99718)
SPONASTRIME dysplasia (Orphanet:93357)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE (OMIM:609223)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Sjögren-Larsson syndrome (Orphanet:816)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)