Spondylolysis

Symptom Information:

Symptom ID: HPO:0003304
Synonyms:
Spondylolysis [OMIM:Spondylolysis]
Spondylolysis [MedDRA:10052013]
Quality:
Cross references:
OMIM: "Spondylolysis" [OMIM:Spondylolysis]
UMLS:C0038018 "Spondylolysis" [HPO:0003304]
Is a (Direct Parents):
HPO         Abnormality of the vertebral column
MedDRA Spine and neck deformities
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)
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)