Vertebral fusion

Symptom Information:

Symptom ID: HPO:0002948
Synonyms:
Fused vertebrae [HPO:0002948]
Fusion of vertebral bodies [HPO:0002948]
Spinal fusion [HPO:0002948]
Vertebral body fusion [HPO:0002948]
Fused vertebrae [OMIM:Fused vertebrae]
Fusion of vertebral bodies [OMIM:Fusion of vertebral bodies]
Spinal fusion [OMIM:Spinal fusion]
Vertebral body fusion [OMIM:Vertebral body fusion]
Vertebral fusion [OMIM:Vertebral fusion]
Fused vertebrae (cervical, thoracic, lumbar) [OMIM:Fused vertebrae (cervical, thoracic, lumbar)]
Vertebral fusion (55%) [OMIM:Vertebral fusion (55%)]
Vertebral fusion (rare) [OMIM:Vertebral fusion (rare)]
Vertebral fusions [OMIM:Vertebral fusions]
Quality:
Cross references:
OMIM: "Fused vertebrae" [OMIM:Fused vertebrae]
OMIM: "Fusion of vertebral bodies" [OMIM:Fusion of vertebral bodies]
OMIM: "Spinal fusion" [OMIM:Spinal fusion]
OMIM: "Vertebral body fusion" [OMIM:Vertebral body fusion]
OMIM: "Vertebral fusion" [OMIM:Vertebral fusion]
OMIM: "Fused vertebrae (cervical, thoracic, lumbar)" [OMIM:Fused vertebrae (cervical, thoracic, lumbar)]
OMIM: "Vertebral fusion (55%)" [OMIM:Vertebral fusion (55%)]
OMIM: "Vertebral fusion (rare)" [OMIM:Vertebral fusion (rare)]
OMIM: "Vertebral fusions" [OMIM:Vertebral fusions]
Is a (Direct Parents):
HPO         Abnormality of the vertebrae
HPO         Synostosis of joints
HPO         Fused lumbar vertebrae
HPO         Sacralization of the fifth lumbar vertebra
HPO         Fused thoracic vertebrae
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)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Synostosis of joints(HPO:0100240)
                      Vertebral fusion(HPO:0002948)
MedDRA:
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

Alkaptonuria (Orphanet:56)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Autosomal dominant multiple pterygium syndrome (Orphanet:65743)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Brachydactyly type B (Orphanet:93383)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Gorlin syndrome (Orphanet:377)
KBG syndrome (Orphanet:2332)
Koolen-De Vries syndrome (Orphanet:96169)
Lateral meningocele syndrome (Orphanet:2789)
Lethal multiple pterygium syndrome (Orphanet:33108)
MELAS (Orphanet:550)
MULTIPLE SYNOSTOSES SYNDROME 2 (OMIM:610017)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Myhre syndrome (Orphanet:2588)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE (OMIM:277300)
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE (OMIM:613686)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
TMCO1 defect syndrome (Orphanet:228407)
VERHEIJ SYNDROME (OMIM:615583)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)