Fused cervical vertebrae
Symptom Information:
Symptom ID: | HPO:0002949 | ||||||
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) 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) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
ASYMMETRIC SHORT STATURE SYNDROME | (OMIM:108450) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Atelosteogenesis type I | (Orphanet:1190) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Cardiospondylocarpofacial syndrome | (Orphanet:3238) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE | (OMIM:214300) |
Okihiro syndrome | (Orphanet:93293) |
Skeletal dysplasia - intellectual deficit | (Orphanet:1436) |
Stapes ankylosis with broad thumbs and toes | (Orphanet:140917) |
Sterile multifocal osteomyelitis with periostitis and pustulosis | (Orphanet:210115) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Wildervanck syndrome | (Orphanet:3456) |