Abnormality of the vertebral column
Symptom Information:
Symptom ID: | HPO:0000925 | ||||||||
Synonyms: |
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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) MedDRA: |
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Database Frequency: | 20 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES | (OMIM:109120) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Anophthalmia plus syndrome | (Orphanet:1104) |
Arachnoid cyst | (Orphanet:2356) |
Autosomal dominant osteopetrosis type 1 | (Orphanet:2783) |
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1 | (OMIM:601884) |
Brachydactyly type A6 | (Orphanet:93382) |
Brachytelephalangic chondrodysplasia punctata | (Orphanet:79345) |
Branchio-skeleto-genital syndrome | (Orphanet:1299) |
CERVICAL VERTEBRAL BRIDGE | (OMIM:118000) |
Chordoma | (Orphanet:178) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Diabetic embryopathy | (Orphanet:1926) |
Hereditary arterial and articular multiple calcification syndrome | (Orphanet:289601) |
Leri pleonosteosis | (Orphanet:2900) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
MURCS association | (Orphanet:2578) |
Neurofibromatosis type 3 | (Orphanet:93921) |
OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE | (OMIM:602475) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |