Thoracolumbar kyphosis

Symptom Information:

Symptom ID: HPO:0005619
Synonyms:
Thoracolumbar gibbus [HPO:0005619]
Thoracolumbar gibbus deformity [HPO:0005619]
Thoracolumbar gibbus [OMIM:Thoracolumbar gibbus]
Thoracolumbar gibbus deformity [OMIM:Thoracolumbar gibbus deformity]
Thoracolumbar kyphosis [OMIM:Thoracolumbar kyphosis]
Quality:
Cross references:
OMIM: "Thoracolumbar gibbus" [OMIM:Thoracolumbar gibbus]
OMIM: "Thoracolumbar gibbus deformity" [OMIM:Thoracolumbar gibbus deformity]
OMIM: "Thoracolumbar kyphosis" [OMIM:Thoracolumbar kyphosis]
Is a (Direct Parents):
HPO         Abnormality of the lumbar spine
HPO         Thoracic kyphosis
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 thorax(HPO:0000765)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic kyphosis(HPO:0002942)
                         Thoracolumbar kyphosis(HPO:0005619)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the curvature of the vertebral column(HPO:0010674)
                      Kyphosis(HPO:0002808)
                         Thoracic kyphosis(HPO:0002942)
                            Thoracolumbar kyphosis(HPO:0005619)
                   Abnormality of the thoracic spine(HPO:0100711)
                      Thoracic kyphosis(HPO:0002942)
                         Thoracolumbar kyphosis(HPO:0005619)
                   Abnormality of the lumbar spine(HPO:0100712)
                      Thoracolumbar kyphosis(HPO:0005619)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Alpha-mannosidosis (Orphanet:61)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Hydrocephaly - tall stature - joint laxity (Orphanet:2181)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 7 (Orphanet:584)
Osteopathia striata - cranial sclerosis (Orphanet:2780)