Cervical C5/C6 vertebrae fusion
Symptom Information:
Symptom ID: | HPO:0004635 | ||
Synonyms: |
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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) Vertebral fusion(HPO:0002948) Fused cervical vertebrae(HPO:0002949) Cervical C5/C6 vertebrae fusion(HPO:0004635) Abnormal joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Synostosis of joints(HPO:0100240) Vertebral fusion(HPO:0002948) Fused cervical vertebrae(HPO:0002949) Cervical C5/C6 vertebrae fusion(HPO:0004635) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Apert syndrome | (Orphanet:87) |
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT | (OMIM:613702) |