Vertebral segmentation defect

Symptom Information:

Symptom ID: HPO:0003422
Synonyms:
Abnormal spinal segmentation [HPO:0003422]
Defect of vertebral segmentation [HPO:0003422]
Abnormal spinal segmentation [OMIM:Abnormal spinal segmentation]
Vertebral segmentation defects [OMIM:Vertebral segmentation defects]
Vertebral segmentation defects (rare) [OMIM:Vertebral segmentation defects (rare)]
Quality:
Cross references:
OMIM: "Abnormal spinal segmentation" [OMIM:Abnormal spinal segmentation]
OMIM: "Vertebral segmentation defects" [OMIM:Vertebral segmentation defects]
OMIM: "Vertebral segmentation defects (rare)" [OMIM:Vertebral segmentation defects (rare)]
Is a (Direct Parents):
HPO         Abnormality of the 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 segmentation defect(HPO:0003422)
MedDRA:
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)