Abnormal form of the vertebral bodies
Symptom Information:
Symptom ID: | HPO:0003312 | |||||||
Synonyms: |
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Quality: | ||||||||
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) Abnormal form of the vertebral bodies(HPO:0003312) MedDRA: |
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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-Küster-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) |