Lumbar hyperlordosis

Symptom Information:

Symptom ID: HPO:0002938
Synonyms:
Exaggerated lumbar lordosis [HPO:0002938]
Increased lumbar lordosis [HPO:0002938]
Lumbar lordosis [HPO:0002938]
Prominent lumbar lordosis [HPO:0002938]
Lordosis [Orphanet:16090]
Lordosis deformity of spine (disorder) [Orphanet:16090]
Exaggerated lumbar lordosis [OMIM:Exaggerated lumbar lordosis]
Increased lumbar lordosis [OMIM:Increased lumbar lordosis]
Lumbar hyperlordosis [OMIM:Lumbar hyperlordosis]
Lumbar lordosis [OMIM:Lumbar lordosis]
Prominent lumbar lordosis [OMIM:Prominent lumbar lordosis]
Lordosis [MedDRA:10024842]
Lordosis (acquired) [MedDRA:10024842]
Lordosis (acquired) (postural) [MedDRA:10024842]
Lordosis associated with other conditions [MedDRA:10024842]
Other lordosis, acquired [MedDRA:10024842]
Lumbar lordosis, increased [OMIM:Lumbar lordosis, increased]
Quality:
Cross references:
HPO:0003307 "Hyperlordosis" [Orphanet:16090]
Orphanet:16090 "Lordosis" [Orphanet:16090]
OMIM: "Exaggerated lumbar lordosis" [OMIM:Exaggerated lumbar lordosis]
OMIM: "Increased lumbar lordosis" [OMIM:Increased lumbar lordosis]
OMIM: "Lumbar hyperlordosis" [OMIM:Lumbar hyperlordosis]
OMIM: "Lumbar lordosis" [OMIM:Lumbar lordosis]
OMIM: "Prominent lumbar lordosis" [OMIM:Prominent lumbar lordosis]
OMIM: "Lumbar lordosis, increased" [OMIM:Lumbar lordosis, increased]
UMLS:C0024003 "Lordosis" [Orphanet:16090]
Is a (Direct Parents):
HPO         Hyperlordosis
MedDRA Spine and neck deformities
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)
                      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)
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)