Hemivertebrae
Symptom Information:
Symptom ID: | HPO:0002937 | ||||||||||
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) Abnormal form of the vertebral bodies(HPO:0003312) Hemivertebrae(HPO:0002937) Vertebral segmentation defect(HPO:0003422) Hemivertebrae(HPO:0002937) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of spine congenital(MedDRA:10028383) Hemivertebrae(HPO:0002937) |
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Database Frequency: | 41 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Aicardi syndrome | (Orphanet:50) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Autosomal dominant multiple pterygium syndrome | (Orphanet:65743) |
Autosomal dominant spondylocostal dysostosis | (Orphanet:1797) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
Brachydactyly type B | (Orphanet:93383) |
Braddock syndrome | (Orphanet:52047) |
CHARGE syndrome | (Orphanet:138) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cloacal exstrophy | (Orphanet:93929) |
Diabetic embryopathy | (Orphanet:1926) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Exstrophy-epispadias complex | (Orphanet:322) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
Femoral-facial syndrome | (Orphanet:1988) |
Goldenhar syndrome | (Orphanet:374) |
Gorlin syndrome | (Orphanet:377) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Incontinentia pigmenti | (Orphanet:464) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
Pallister-Hall syndrome | (Orphanet:672) |
Peters-plus syndrome | (Orphanet:709) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Poland syndrome | (Orphanet:2911) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE | (OMIM:277300) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Sprengel deformity | (Orphanet:3181) |
VERHEIJ SYNDROME | (OMIM:615583) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |