Spinal canal stenosis

Symptom Information:

Symptom ID: HPO:0003416
Synonyms:
Narrow spinal canal [HPO:0003416]
Spinal stenosis [HPO:0003416]
Spine canal stenosis [Orphanet:16240]
Spinal stenosis (disorder) [Orphanet:16240]
Spinal Stenosis [Orphanet:16240]
Narrow spinal canal [OMIM:Narrow spinal canal]
Spinal canal stenosis [OMIM:Spinal canal stenosis]
Spinal stenosis [OMIM:Spinal stenosis]
Rachidian/spine canal stenosis [Orphanet:16240]
Spinal stenosis NOS [Orphanet:16240]
Spinal column stenosis [MedDRA:10041540]
Spinal stenosis NOS [MedDRA:10041540]
Spinal stenosis of other region [MedDRA:10041540]
Spinal stenosis of thoracic region [MedDRA:10041540]
Spinal stenosis of unspecified region [MedDRA:10041540]
Spinal stenosis, other than cervical [MedDRA:10041540]
Spinal stenoses [OMIM:Spinal stenoses]
Quality:
Cross references:
Orphanet:16240 "Rachidian/spine canal stenosis" [Orphanet:16240]
OMIM: "Narrow spinal canal" [OMIM:Narrow spinal canal]
OMIM: "Spinal canal stenosis" [OMIM:Spinal canal stenosis]
OMIM: "Spinal stenosis" [OMIM:Spinal stenosis]
OMIM: "Spinal stenoses" [OMIM:Spinal stenoses]
UMLS:C0037944 "Spinal Stenosis" [Orphanet:16240]
Is a (Direct Parents):
MedDRA Spinal cord and nerve root disorders NEC
HPO         Abnormality of the vertebral column
Orphanet Abnormality of the vertebral column
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)
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)