Abnormality of the cervical spine

Symptom Information:

Symptom ID: HPO:0003319
Synonyms:
Abnormal cervical spine [HPO:0003319]
Abnormality of the cervical vertebrae [HPO:0003319]
Cervical spine abnormalities [HPO:0003319]
Cervical vertebral abnormalities [HPO:0003319]
CERVICAL VERTEBRAL ANOMALIES [HPO:0003319]
Abnormal cervical spine [OMIM:Abnormal cervical spine]
Cervical spine abnormalities [OMIM:Cervical spine abnormalities]
Cervical vertebral abnormalities [OMIM:Cervical vertebral abnormalities]
Cervical vertebral anomalies [OMIM:Cervical vertebral anomalies]
Quality:
Cross references:
OMIM: "Abnormal cervical spine" [OMIM:Abnormal cervical spine]
OMIM: "Cervical spine abnormalities" [OMIM:Cervical spine abnormalities]
OMIM: "Cervical vertebral abnormalities" [OMIM:Cervical vertebral abnormalities]
OMIM: "Cervical vertebral anomalies" [OMIM:Cervical vertebral anomalies]
Is a (Direct Parents):
HPO         Abnormality of the vertebral column
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 cervical spine(HPO:0003319)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

CERVICAL CANCER (OMIM:603956)
Crouzon disease (Orphanet:207)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Nager syndrome (Orphanet:245)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)