Spondylolysis
Symptom Information:
Symptom ID: | HPO:0003304 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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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) Spondylolysis(HPO:0003304) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Spine and neck deformities(MedDRA:10012140) Spondylolysis(HPO:0003304) |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
Cleidocranial dysplasia | (Orphanet:1452) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Pycnodysostosis | (Orphanet:763) |
SPONDYLOLISTHESIS | (OMIM:184200) |
SPONDYLOSIS, CERVICAL | (OMIM:184300) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |