Thoracic scoliosis

Symptom Information:

Symptom ID: HPO:0002943
Synonyms:
Thoracic scoliosis [OMIM:Thoracic scoliosis]
Quality:
Cross references:
OMIM: "Thoracic scoliosis" [OMIM:Thoracic scoliosis]
Is a (Direct Parents):
HPO         Abnormality of the thoracic spine
HPO         Scoliosis
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 curvature of the vertebral column(HPO:0010674)
                      Scoliosis(HPO:0002650)
                         Thoracic scoliosis(HPO:0002943)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic scoliosis(HPO:0002943)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic scoliosis(HPO:0002943)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
Cohen syndrome (Orphanet:193)
Ectodermal dysplasia - sensorineural deafness (Orphanet:1883)
GCS1-CDG (Orphanet:79330)
Holt-Oram syndrome (Orphanet:392)
Jawad syndrome (Orphanet:313795)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Noonan syndrome (Orphanet:648)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Pseudoaminopterin syndrome (Orphanet:221120)