Kyphosis
Symptom Information:
Symptom ID: | HPO:0002808 | |||||||||||||||||||
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 curvature of the vertebral column(HPO:0010674) Kyphosis(HPO:0002808) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Spine and neck deformities(MedDRA:10012140) Kyphosis(HPO:0002808) |
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Database Frequency: | 289 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q12 microdeletion syndrome | (Orphanet:261144) |
15q14 microdeletion syndrome | (Orphanet:261190) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
3C syndrome | (Orphanet:7) |
3M syndrome | (Orphanet:2616) |
4q21 microdeletion syndrome | (Orphanet:238750) |
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
Achondroplasia | (Orphanet:15) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acromegaly | (Orphanet:963) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alexander disease | (Orphanet:58) |
Alkaptonuria | (Orphanet:56) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alpha-mannosidosis | (Orphanet:61) |
Alström syndrome | (Orphanet:64) |
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Arthrogryposis due to muscular dystrophy | (Orphanet:1155) |
Aspartylglucosaminuria | (Orphanet:93) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal dominant brachyolmia | (Orphanet:93304) |
Autosomal dominant congenital benign spinal muscular atrophy | (Orphanet:1216) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive spastic paraplegia type 18 | (Orphanet:209951) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 53 | (Orphanet:319199) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
BRUCK SYNDROME 1 | (OMIM:259450) |
Becker nevus syndrome | (Orphanet:64755) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachyolmia | (Orphanet:1293) |
Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Bruck syndrome | (Orphanet:2771) |
CHILD syndrome | (Orphanet:139) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
CK syndrome | (Orphanet:251383) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cabezas syndrome | (Orphanet:85293) |
Campomelic dysplasia | (Orphanet:140) |
Camurati-Engelmann disease | (Orphanet:1328) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Classical homocystinuria | (Orphanet:394) |
Cleidocranial dysplasia | (Orphanet:1452) |
Cockayne syndrome | (Orphanet:191) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Congenital muscular dystrophy - infantile cataract - hypogonadism | (Orphanet:1875) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Cowden syndrome | (Orphanet:201) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
Cushing disease | (Orphanet:96253) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT | (OMIM:128100) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Desbuquois syndrome | (Orphanet:1425) |
Developmental malformations - deafness - dystonia | (Orphanet:79107) |
Diastrophic dwarfism | (Orphanet:628) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Dysostosis, Stanescu type | (Orphanet:1798) |
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609944) |
Early-onset generalized limb-onset dystonia | (Orphanet:256) |
Ectodermal dysplasia - sensorineural deafness | (Orphanet:1883) |
Ehlers-Danlos syndrome type 7A | (Orphanet:99875) |
Ehlers-Danlos syndrome type 7B | (Orphanet:99876) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Emanuel syndrome | (Orphanet:96170) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
FACES syndrome | (Orphanet:1969) |
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C | (OMIM:609384) |
Familial Scheuermann disease | (Orphanet:3135) |
Familial osteodysplasia, Anderson type | (Orphanet:2769) |
Farber lipogranulomatosis | (Orphanet:333) |
Flynn-Aird syndrome | (Orphanet:2047) |
Fountain syndrome | (Orphanet:3219) |
Friedreich ataxia 1 | (OMIM:229300) |
Fucosidosis | (Orphanet:349) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
GM1 gangliosidosis type 3 | (Orphanet:79257) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
Hall-Riggs syndrome | (Orphanet:2107) |
Harrod syndrome | (Orphanet:2115) |
Heart defects - limb shortening | (Orphanet:1354) |
Hip dysplasia, Beukes type | (Orphanet:2114) |
Horizontal gaze palsy with progressive scoliosis | (Orphanet:2744) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Ichthyosis-cheek-eyebrow syndrome | (Orphanet:2267) |
Idiopathic juvenile osteoporosis | (Orphanet:85193) |
Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration | (Orphanet:85317) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Ito hypomelanosis | (Orphanet:435) |
Kniest dysplasia | (Orphanet:485) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lateral meningocele syndrome | (Orphanet:2789) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Lethal chondrodysplasia, Moerman type | (Orphanet:1420) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Limb body wall complex | (Orphanet:2369) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MASA syndrome | (Orphanet:2466) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 | (OMIM:615761) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 | (OMIM:615834) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 | (OMIM:300676) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Marden-Walker syndrome | (Orphanet:2461) |
Marfan syndrome | (Orphanet:558) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
McCune-Albright syndrome | (Orphanet:562) |
McDonough syndrome | (Orphanet:2471) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Metatropic dysplasia | (Orphanet:2635) |
Micro syndrome | (Orphanet:2510) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
Microphthalmia, Lenz type | (Orphanet:568) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Monosomy 9q22.3 | (Orphanet:77301) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
Multiple non-ossifying fibromatosis | (Orphanet:2029) |
Neurofibromatosis type 1 | (Orphanet:636) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
OSTEOGENESIS IMPERFECTA, TYPE IV | (OMIM:166220) |
OSTEOGENESIS IMPERFECTA, TYPE IX | (OMIM:259440) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
Occipital horn syndrome | (Orphanet:198) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa | (Orphanet:2653) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
Osteogenesis imperfecta type 4 | (Orphanet:216820) |
Osteomesopyknosis | (Orphanet:2777) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
PELGER-HUET ANOMALY | (OMIM:169400) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 | (OMIM:610489) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 | (OMIM:610475) |
PMM2-CDG | (Orphanet:79318) |
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED | (OMIM:177850) |
Parastremmatic dwarfism | (Orphanet:2646) |
Pelizaeus-Merzbacher disease | (Orphanet:702) |
Pelvis-shoulder dysplasia | (Orphanet:2839) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Prader-Willi syndrome | (Orphanet:739) |
Primary hypergonadotropic hypogonadism - partial alopecia | (Orphanet:2232) |
Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Progressive hemifacial atrophy | (Orphanet:1214) |
Progressive non-infectious anterior vertebral fusion | (Orphanet:2062) |
Progressive pseudorheumatoid arthropathy of childhood | (Orphanet:1159) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Pseudoachondroplasia | (Orphanet:750) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pycnodysostosis | (Orphanet:763) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Ramon syndrome | (Orphanet:3019) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Rett syndrome | (Orphanet:778) |
Rhizomelic syndrome, Urbach type | (Orphanet:3098) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Richieri Costa-da Silva syndrome | (Orphanet:3101) |
Ruvalcaba syndrome | (Orphanet:3121) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
SPONASTRIME dysplasia | (Orphanet:93357) |
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:106300) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED | (OMIM:313400) |
STICKLER SYNDROME, TYPE I | (OMIM:108300) |
Sandhoff disease | (Orphanet:796) |
Scheie syndrome | (Orphanet:93474) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Shoulder and thorax deformity - congenital heart disease | (Orphanet:1940) |
Sialidosis type 1 | (Orphanet:812) |
Sialidosis type 2 | (Orphanet:87876) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Skeletal dysplasia - epilepsy - short stature | (Orphanet:1858) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Smith-McCort dysplasia | (Orphanet:178355) |
Spastic paraplegia-optic atrophy-neuropathy syndrome | (Orphanet:320406) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloenchondrodysplasia | (Orphanet:1855) |
Spondyloepimetaphyseal dysplasia congenita, Strudwick type | (Orphanet:93346) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia tarda | (Orphanet:93284) |
Spondylometaphyseal dysplasia, 'corner fracture' type | (Orphanet:93315) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
Spondylometaphyseal dysplasia, Schmidt type | (Orphanet:93316) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
Stickler syndrome | (Orphanet:828) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Thanatophoric dysplasia | (Orphanet:2655) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
Thanatophoric dysplasia type 2 | (Orphanet:93274) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |
Trisomy 13 | (Orphanet:3378) |
Trisomy 9p | (Orphanet:236) |
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME | (OMIM:300280) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
WIDOW'S PEAK SYNDROME | (OMIM:314570) |
Weaver syndrome | (Orphanet:3447) |
Weismann-Netter syndrome | (Orphanet:3344) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |