Vertebral fusion
Symptom Information:
Symptom ID: | HPO:0002948 | |||||||||||||
Synonyms: |
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Cross references: |
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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) Abnormal joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Synostosis of joints(HPO:0100240) Vertebral fusion(HPO:0002948) MedDRA: |
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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) |