Fused cervical vertebrae

Symptom Information:

Symptom ID: HPO:0002949
Synonyms:
Cervical vertebral fusion [HPO:0002949]
Fusion of cervical vertebrae [HPO:0002949]
Cervical vertebral fusion [OMIM:Cervical vertebral fusion]
Fused cervical vertebrae [OMIM:Fused cervical vertebrae]
Fusion of cervical vertebrae [OMIM:Fusion of cervical vertebrae]
Cervical vertebral fusion (in some patients) [OMIM:Cervical vertebral fusion (in some patients)]
Quality:
Cross references:
OMIM: "Cervical vertebral fusion" [OMIM:Cervical vertebral fusion]
OMIM: "Fused cervical vertebrae" [OMIM:Fused cervical vertebrae]
OMIM: "Fusion of cervical vertebrae" [OMIM:Fusion of cervical vertebrae]
OMIM: "Cervical vertebral fusion (in some patients)" [OMIM:Cervical vertebral fusion (in some patients)]
Is a (Direct Parents):
HPO         Cervical C3/C4 vertebral fusion
HPO         Vertebral fusion
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:
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)