Hemivertebrae

Symptom Information:

Symptom ID: HPO:0002937
Synonyms:
Hemivertebra [HPO:0002937]
Hemivertebra [Orphanet:16540]
Congenital hemivertebra [HPO:0002937]
Congenital hemivertebra (disorder) [Orphanet:16540]
Congenital hemivertebra [Orphanet:16540]
Hemivertebra [OMIM:Hemivertebra]
Hemivertebrae [OMIM:Hemivertebrae]
Vertebral segmentation anomaly/hemivertebrae [Orphanet:16540]
Hemivertebra [MedDRA:10019477]
Hemivertebrae (in some patients) [OMIM:Hemivertebrae (in some patients)]
Quality:
Cross references:
Orphanet:16540 "Vertebral segmentation anomaly/hemivertebrae" [Orphanet:16540]
OMIM: "Hemivertebra" [OMIM:Hemivertebra]
OMIM: "Hemivertebrae" [OMIM:Hemivertebrae]
OMIM: "Hemivertebrae (in some patients)" [OMIM:Hemivertebrae (in some patients)]
UMLS:C0265677 "Hemivertebrae" [HPO:0002937]
UMLS:C0265677 "Congenital hemivertebra" [Orphanet:16540]
Is a (Direct Parents):
HPO         Abnormal form of the vertebral bodies
HPO         Vertebral segmentation defect
Orphanet Abnormality of the vertebral column
MedDRA Musculoskeletal and connective tissue disorders of spine congenital
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 segmentation defect(HPO:0003422)
                         Hemivertebrae(HPO:0002937)
                      Abnormal form of the vertebral bodies(HPO:0003312)
                         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)
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)