Back pain
Symptom Information:
| Symptom ID: | HPO:0003418 | ||||
| Synonyms: |
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| 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) Back pain(HPO:0003418) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders NEC(MedDRA:10028393) Musculoskeletal and connective tissue pain and discomfort(MedDRA:10068757) Back pain(HPO:0003418) |
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| Database Frequency: | 17 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Alkaptonuria | (Orphanet:56) |
| Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
| Brachyolmia type 1, Toledo type | (Orphanet:93303) |
| Caudal regression sequence | (Orphanet:3027) |
| Familial caudal dysgenesis | (Orphanet:1768) |
| Hurler syndrome | (Orphanet:93473) |
| Hurler-Scheie syndrome | (Orphanet:93476) |
| Hypouricemia, renal, 1 | (OMIM:220150) |
| INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
| Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
| Isolated polycystic liver disease | (Orphanet:2924) |
| Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
| SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:106300) |
| Scheie syndrome | (Orphanet:93474) |
| Sirenomelia | (Orphanet:3169) |
| Wilson disease | (Orphanet:905) |
| X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |