Lumbar hyperlordosis
Symptom Information:
Symptom ID: | HPO:0002938 | |||||||||||||||||
Synonyms: |
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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) Hyperlordosis(HPO:0003307) Lumbar hyperlordosis(HPO:0002938) 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) Lumbar hyperlordosis(HPO:0002938) |
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Database Frequency: | 73 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondroplasia | (Orphanet:15) |
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Atelosteogenesis type II | (Orphanet:56304) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive limb-girdle muscular dystrophy type 2P | (Orphanet:280333) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
COLD-INDUCED SWEATING SYNDROME 2 | (OMIM:610313) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cohen syndrome | (Orphanet:193) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED | (OMIM:304950) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Fucosidosis | (Orphanet:349) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Gordon syndrome | (Orphanet:376) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypochondroplasia | (Orphanet:429) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
Langer mesomelic dysplasia | (Orphanet:2632) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Multiple epiphyseal dysplasia, with miniepiphyses | (Orphanet:166032) |
Myosclerosis | (Orphanet:289380) |
Nail-patella syndrome | (Orphanet:2614) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
Pelvis-shoulder dysplasia | (Orphanet:2839) |
Pseudoachondroplasia | (Orphanet:750) |
Pseudodiastrophic dysplasia | (Orphanet:85174) |
SPONASTRIME dysplasia | (Orphanet:93357) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT | (OMIM:184100) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE | (OMIM:609223) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED | (OMIM:313400) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Spondyloenchondrodysplasia | (Orphanet:1855) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondyloepimetaphyseal dysplasia, aggrecan type | (Orphanet:171866) |
Spondyloepimetaphyseal dysplasia, matrilin-3 type | (Orphanet:156728) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia tarda | (Orphanet:93284) |
Spondyloepiphyseal dysplasia, MacDermot type | (Orphanet:163668) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
Spondylometaphyseal dysplasia, Schmidt type | (Orphanet:93316) |
Stiff person syndrome | (Orphanet:3198) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome | (Orphanet:85295) |