Kyphosis

Symptom Information:

Symptom ID: HPO:0002808
Synonyms:
Gibbus deformity [HPO:0002808]
Hyperkyphosis [HPO:0002808]
Round back [HPO:0002808]
Kyphosis deformity of spine [HPO:0002808]
Kyphosis deformity of spine (disorder) [Orphanet:16060]
Kyphosis deformity of spine [Orphanet:16060]
Gibbus deformity [OMIM:Gibbus deformity]
Hyperkyphosis [OMIM:Hyperkyphosis]
Kyphosis [OMIM:Kyphosis]
Kyphosis [Orphanet:16060]
Kyphosis [MedDRA:10023509]
Adolescent postural kyphosis [MedDRA:10023509]
Hunchback (acquired) [MedDRA:10023509]
Kyphosis (acquired) [MedDRA:10023509]
Kyphosis (acquired) (postural) [MedDRA:10023509]
Kyphosis associated with other conditions [MedDRA:10023509]
Other kyphosis, acquired [MedDRA:10023509]
Kyphosis (in some patients) [OMIM:Kyphosis (in some patients)]
Kyphosis (onset 3-6 months) [OMIM:Kyphosis (onset 3-6 months)]
Quality:
Cross references:
Orphanet:16060 "Kyphosis" [Orphanet:16060]
OMIM: "Gibbus deformity" [OMIM:Gibbus deformity]
OMIM: "Hyperkyphosis" [OMIM:Hyperkyphosis]
OMIM: "Kyphosis" [OMIM:Kyphosis]
OMIM: "Kyphosis (in some patients)" [OMIM:Kyphosis (in some patients)]
OMIM: "Kyphosis (onset 3-6 months)" [OMIM:Kyphosis (onset 3-6 months)]
UMLS:C0265673 "Kyphosis" [HPO:0002808]
UMLS:C1845112 "Hyperkyphosis" [HPO:0002808]
UMLS:C0022821 "Kyphosis deformity of spine" [Orphanet:16060]
Is a (Direct Parents):
MedDRA Spine and neck deformities
HPO         Abnormality of the curvature of the vertebral column
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 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)
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)