Thoracic scoliosis
Symptom Information:
Symptom ID: | HPO:0002943 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |