Thoracic kyphosis
Symptom Information:
Symptom ID: | HPO:0002942 | |||||
Synonyms: |
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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 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) Abnormality of the thorax(HPO:0000765) Abnormality of the thoracic spine(HPO:0100711) Thoracic kyphosis(HPO:0002942) MedDRA: |
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Database Frequency: | 14 / 7739 | |||||
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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) |