Vertebral segmentation defect
Symptom Information:
Symptom ID: | HPO:0003422 | |||||
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 segmentation defect(HPO:0003422) MedDRA: |
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Database Frequency: | 95 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
1q41q42 microdeletion syndrome | (Orphanet:250999) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
3C syndrome | (Orphanet:7) |
3q29 microdeletion syndrome | (Orphanet:65286) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Aicardi syndrome | (Orphanet:50) |
Alagille syndrome | (Orphanet:52) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Anophthalmia plus syndrome | (Orphanet:1104) |
Apert syndrome | (Orphanet:87) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant spondylocostal dysostosis | (Orphanet:1797) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
BRESEK syndrome | (Orphanet:85284) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
CHARGE syndrome | (Orphanet:138) |
COG1-CDG | (Orphanet:263508) |
Camptodactyly - joint contractures - facial skeletal defects | (Orphanet:1323) |
Cardiospondylocarpofacial syndrome | (Orphanet:3238) |
Caudal duplication | (Orphanet:1756) |
Caudal regression sequence | (Orphanet:3027) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Cloacal exstrophy | (Orphanet:93929) |
Congenital unilateral hypoplasia of depressor anguli oris | (Orphanet:1166) |
Craniosynostosis - fibular aplasia | (Orphanet:1533) |
DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA | (OMIM:221950) |
Diabetic embryopathy | (Orphanet:1926) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Distal monosomy 6p | (Orphanet:96125) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
Dysspondyloenchondromatosis | (Orphanet:85198) |
Embryonary disorganization syndrome | (Orphanet:1664) |
Femoral-facial syndrome | (Orphanet:1988) |
Fetal alcohol syndrome | (Orphanet:1915) |
Fraser syndrome | (Orphanet:2052) |
Goldenhar syndrome | (Orphanet:374) |
Gorlin syndrome | (Orphanet:377) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Isolated spina bifida | (Orphanet:823) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lethal chondrodysplasia, Moerman type | (Orphanet:1420) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
MURCS association | (Orphanet:2578) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
Mesomelic dysplasia, Kantaputra type | (Orphanet:1836) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Micromelic dwarfism, Fryns type | (Orphanet:2641) |
Mirror polydactyly - vertebral segmentation - limbs defects | (Orphanet:3004) |
Mosaic trisomy 8 | (Orphanet:96061) |
Mosaic trisomy 9 | (Orphanet:99776) |
Nevus comedonicus syndrome | (Orphanet:64754) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PHAVER syndrome | (Orphanet:2876) |
Peters-plus syndrome | (Orphanet:709) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Posterior fusion of lumbosacral vertebrae - blepharoptosis | (Orphanet:2064) |
Prata-Liberal-Goncalves syndrome | (Orphanet:2956) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Prune belly syndrome | (Orphanet:2970) |
RAPADILINO syndrome | (Orphanet:3021) |
SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE | (OMIM:608681) |
SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE | (OMIM:609813) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Skeletal dysplasia - intellectual deficit | (Orphanet:1436) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Symbrachydactyly of hands and feet | (Orphanet:1570) |
Syngnathia multiple anomalies | (Orphanet:3262) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Toriello-Carey syndrome | (Orphanet:3338) |
Tracheo-esophageal fistula - hypospadias | (Orphanet:2042) |
Trisomy 20p | (Orphanet:261318) |
VACTERL with hydrocephalus | (Orphanet:3412) |
VACTERL/VATER association | (Orphanet:887) |
Wildervanck syndrome | (Orphanet:3456) |
Williams syndrome | (Orphanet:904) |