Ovoid vertebral bodies
Symptom Information:
Symptom ID: | HPO:0003300 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |