Abnormal form of the vertebral bodies

Symptom Information:

Symptom ID: HPO:0003312
Synonyms:
Abnormally-shaped vertebrae [HPO:0003312]
Round vertebral bodies [HPO:0003312]
Vertebra shape anomaly [Orphanet:16270]
Abnormally-shaped vertebrae [OMIM:Abnormally-shaped vertebrae]
Round vertebral bodies [OMIM:Round vertebral bodies]
Abnormal vertebral size/shape [Orphanet:16270]
Vertebra size anomaly [Orphanet:16270]
Quality:
Cross references:
Orphanet:16270 "Abnormal vertebral size/shape" [Orphanet:16270]
OMIM: "Abnormally-shaped vertebrae" [OMIM:Abnormally-shaped vertebrae]
OMIM: "Round vertebral bodies" [OMIM:Round vertebral bodies]
Is a (Direct Parents):
HPO         Abnormality of the vertebrae
Orphanet Abnormality of the vertebral column
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)
MedDRA:
Database Frequency: 172 / 7739
Resource:

All diseases associated with this symptom:

17q12 microduplication syndrome (Orphanet:261272)
3M syndrome (Orphanet:2616)
Achondroplasia (Orphanet:15)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocapitofemoral dysplasia (Orphanet:63446)
Acrocraniofacial dysostosis (Orphanet:949)
Acrodysostosis (Orphanet:950)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Acroosteolysis, dominant type (Orphanet:955)
Alagille syndrome (Orphanet:52)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Arthrogryposis-like syndrome (Orphanet:1149)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant brachyolmia (Orphanet:93304)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Autosomal recessive Stickler syndrome (Orphanet:250984)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Blepharophimosis - radioulnar synostosis (Orphanet:1256)
Brachydactylous dwarfism, Mseleni type (Orphanet:2619)
Brachyolmia, Maroteaux type (Orphanet:93302)
Braddock syndrome (Orphanet:52047)
CODAS syndrome (Orphanet:1458)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Coffin-Lowry syndrome (Orphanet:192)
Cole-Carpenter syndrome (Orphanet:2050)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital amegakaryocytic thrombocytopenia (Orphanet:3319)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniolenticulosutural dysplasia (Orphanet:50814)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Diastrophic dwarfism (Orphanet:628)
Distal monosomy 13q (Orphanet:1590)
Distal monosomy 17q (Orphanet:1597)
Duane retraction syndrome (Orphanet:233)
Dysosteosclerosis (Orphanet:1782)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Familial Scheuermann disease (Orphanet:3135)
Familial caudal dysgenesis (Orphanet:1768)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Feingold syndrome (Orphanet:1305)
Fibrochondrogenesis (Orphanet:2021)
Frontometaphyseal dysplasia (Orphanet:1826)
Fucosidosis (Orphanet:349)
GM1 gangliosidosis (Orphanet:354)
Geleophysic dysplasia (Orphanet:2623)
Geroderma osteodysplastica (Orphanet:2078)
Ghosal hematodiaphyseal dysplasia (Orphanet:1802)
Goldenhar syndrome (Orphanet:374)
Gorlin syndrome (Orphanet:377)
Greenberg dysplasia (Orphanet:1426)
Heart defects - limb shortening (Orphanet:1354)
Holoprosencephaly (Orphanet:2162)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypochondroplasia (Orphanet:429)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Jacobsen syndrome (Orphanet:2308)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
KBG syndrome (Orphanet:2332)
Kabuki syndrome (Orphanet:2322)
Kozlowski-Brown-Hardwick syndrome (Orphanet:2352)
Kyphomelic dysplasia (Orphanet:1801)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia (Orphanet:2005)
Lateral meningocele syndrome (Orphanet:2789)
Lathosterolosis (Orphanet:46059)
Leri pleonosteosis (Orphanet:2900)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Limb body wall complex (Orphanet:2369)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Marden-Walker syndrome (Orphanet:2461)
Maxillo-nasal dysplasia (Orphanet:1248)
Mayer-Rokitansky-K├╝ster-Hauser syndrome (Orphanet:3109)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Metatropic dysplasia (Orphanet:2635)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Microphthalmia with limb anomalies (Orphanet:1106)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Multiple epiphyseal dysplasia (Orphanet:251)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Neuronal intranuclear inclusion disease (Orphanet:2289)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Oculodentodigital dysplasia (Orphanet:2710)
Opsismodysplasia (Orphanet:2746)
Osteocraniostenosis (Orphanet:2763)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta (Orphanet:666)
Osteoglophonic dwarfism (Orphanet:2645)
Osteomesopyknosis (Orphanet:2777)
Osteopetrosis (Orphanet:2781)
Osteoporosis - pseudoglioma (Orphanet:2788)
Otopalatodigital syndrome (Orphanet:669)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PHAVER syndrome (Orphanet:2876)
Pallister-Hall syndrome (Orphanet:672)
Pelvis-shoulder dysplasia (Orphanet:2839)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Posterior fusion of lumbosacral vertebrae - blepharoptosis (Orphanet:2064)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Proteus syndrome (Orphanet:744)
Pseudodiastrophic dysplasia (Orphanet:85174)
Pyle disease (Orphanet:3005)
Radio-renal syndrome (Orphanet:3015)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Richieri Costa-da Silva syndrome (Orphanet:3101)
Robin sequence - oligodactyly (Orphanet:3104)
SCARF syndrome (Orphanet:3134)
Saethre-Chotzen syndrome (Orphanet:794)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Schneckenbecken dysplasia (Orphanet:3144)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sialidosis type 1 (Orphanet:812)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Skeletal dysplasia - epilepsy - short stature (Orphanet:1858)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloenchondrodysplasia (Orphanet:1855)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia (Orphanet:253)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia, Kimberley type (Orphanet:93283)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Stickler syndrome (Orphanet:828)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Trisomy 20p (Orphanet:261318)
Ulbright-Hodes syndrome (Orphanet:3404)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
Weaver-Williams syndrome (Orphanet:3448)
Weismann-Netter syndrome (Orphanet:3344)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
Zimmermann-Laband syndrome (Orphanet:3473)