Ovoid vertebral bodies

Symptom Information:

Symptom ID: HPO:0003300
Synonyms:
Bullet vertebral body [HPO:0003300]
Oval vertebral bodies [HPO:0003300]
Ovoid vertebrae [HPO:0003300]
Ovoid-shaped vertebral bodies [HPO:0003300]
Oval vertebral bodies [OMIM:Oval vertebral bodies]
Ovoid vertebrae [OMIM:Ovoid vertebrae]
Ovoid vertebral bodies [OMIM:Ovoid vertebral bodies]
Oval vertebral bodies (infancy) [OMIM:Oval vertebral bodies (infancy)]
Ovoid vertebrae (infancy) [OMIM:Ovoid vertebrae (infancy)]
Ovoid vertebral bodies (infancy) [OMIM:Ovoid vertebral bodies (infancy)]
Ovoid-shaped vertebral bodies (childhood) [OMIM:Ovoid-shaped vertebral bodies (childhood)]
Quality:
Cross references:
OMIM: "Oval vertebral bodies" [OMIM:Oval vertebral bodies]
OMIM: "Ovoid vertebrae" [OMIM:Ovoid vertebrae]
OMIM: "Ovoid vertebral bodies" [OMIM:Ovoid vertebral bodies]
OMIM: "Oval vertebral bodies (infancy)" [OMIM:Oval vertebral bodies (infancy)]
OMIM: "Ovoid vertebrae (infancy)" [OMIM:Ovoid vertebrae (infancy)]
OMIM: "Ovoid vertebral bodies (infancy)" [OMIM:Ovoid vertebral bodies (infancy)]
OMIM: "Ovoid-shaped vertebral bodies (childhood)" [OMIM:Ovoid-shaped vertebral bodies (childhood)]
Is a (Direct Parents):
HPO         Abnormal form of the vertebral bodies
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)
                   Abnormality of the vertebrae(HPO:0003468)
                      Abnormal form of the vertebral bodies(HPO:0003312)
                         Ovoid vertebral bodies(HPO:0003300)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Acrocapitofemoral dysplasia (Orphanet:63446)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Acromicric dysplasia (Orphanet:969)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE (OMIM:611702)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Schneckenbecken dysplasia (Orphanet:3144)
Shwachman-Diamond syndrome (Orphanet:811)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)