Spondylolisthesis

Symptom Information:

Symptom ID: HPO:0003302
Synonyms:
Spondylolithesis [HPO:0003302]
Spondylolisthesis [OMIM:Spondylolisthesis]
Spondylolisthesis (rare) [OMIM:Spondylolisthesis (rare)]
Spondylolisthesis [MedDRA:10063550]
Quality:
Cross references:
OMIM: "Spondylolisthesis" [OMIM:Spondylolisthesis]
OMIM: "Spondylolisthesis (rare)" [OMIM:Spondylolisthesis (rare)]
UMLS:C0038016 "Spondylolisthesis" [HPO:0003302]
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)
                   Spondylolisthesis(HPO:0003302)
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)
          Spondylolisthesis(HPO:0003302)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Alpha-mannosidosis (Orphanet:61)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant multiple pterygium syndrome (Orphanet:65743)
BRITTLE CORNEA SYNDROME 1 (OMIM:229200)
Brittle cornea syndrome (Orphanet:90354)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
Cleidocranial dysplasia (Orphanet:1452)
Koolen-De Vries syndrome (Orphanet:96169)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
Marfan syndrome type 1 (Orphanet:284963)
Pycnodysostosis (Orphanet:763)
RIENHOFF SYNDROME (OMIM:615582)
SPONDYLOSIS, CERVICAL (OMIM:184300)