Spinal canal stenosis
Symptom Information:
Symptom ID: | HPO:0003416 | |||||||||||||||||
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) Spinal canal stenosis(HPO:0003416) MedDRA: Nervous system disorders(MedDRA:10029205) Spinal cord and nerve root disorders(MedDRA:10041543) Spinal cord and nerve root disorders NEC(MedDRA:10041544) Spinal canal stenosis(HPO:0003416) |
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Database Frequency: | 28 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
Achondroplasia | (Orphanet:15) |
Acrodysostosis | (Orphanet:950) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromegaly | (Orphanet:963) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
Brachyolmia type 1, Toledo type | (Orphanet:93303) |
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA | (OMIM:616007) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypochondroplasia | (Orphanet:429) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
Marshall-Smith syndrome | (Orphanet:561) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Multiple synostoses syndrome | (Orphanet:3237) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Proteus syndrome | (Orphanet:744) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Stickler syndrome | (Orphanet:828) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |
X-linked hypophosphatemia | (Orphanet:89936) |