Spinal cord compression
Symptom Information:
Symptom ID: | HPO:0002176 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Spinal cord and nerve root disorders(MedDRA:10041543) Spinal cord and nerve root disorders NEC(MedDRA:10041544) Spinal cord compression(HPO:0002176) |
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Database Frequency: | 15 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant brachyolmia | (Orphanet:93304) |
Brachyolmia | (Orphanet:1293) |
Diastrophic dwarfism | (Orphanet:628) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
Neuroblastoma | (Orphanet:635) |
OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE | (OMIM:602475) |
Proteus syndrome | (Orphanet:744) |
SECKEL SYNDROME 8 | (OMIM:615807) |
Scheie syndrome | (Orphanet:93474) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
X-linked hypophosphatemia | (Orphanet:89936) |