Abnormality of the vertebral column

Symptom Information:

Symptom ID: HPO:0000925
Synonyms:
Abnormal vertebral column [HPO:0000925]
Abnormality of the backbone [HPO:0000925]
Abnormality of the spine [HPO:0000925]
Spine anomaly [Orphanet:16000]
Congenital anomaly of spine (disorder) [Orphanet:16000]
Congenital anomaly of spine [Orphanet:16000]
Abnormal vertebral column [OMIM:Abnormal vertebral column]
Anomalies of spine, vertebrae and pelvis [Orphanet:16000]
Quality:
Cross references:
Orphanet:16000 "Anomalies of spine, vertebrae and pelvis" [Orphanet:16000]
OMIM: "Abnormal vertebral column" [OMIM:Abnormal vertebral column]
UMLS:C0158775 "Congenital anomaly of spine" [Orphanet:16000]
Is a (Direct Parents):
HPO         Neural tube defect
HPO         Abnormal axial skeleton morphology
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:
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)