Hyperlordosis

Symptom Information:

Symptom ID: HPO:0003307
Synonyms:
Lordosis [HPO:0003307]
Lordosis [Orphanet:16090]
Lordosis deformity of spine [HPO:0003307]
Lordosis deformity of spine (disorder) [Orphanet:16090]
lordosis [HPO:0003307]
Hyperlordosis [OMIM:Hyperlordosis]
Lordosis [OMIM: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]
Hyperlordosis (in some patients) [OMIM:Hyperlordosis (in some patients)]
Increased lordosis [OMIM,du]
Quality:
Cross references:
HPO:0002938 "Lumbar hyperlordosis" [Orphanet:16090]
Orphanet:16090 "Lordosis" [Orphanet:16090]
OMIM: "Hyperlordosis" [OMIM:Hyperlordosis]
OMIM: "Lordosis" [OMIM:Lordosis]
OMIM: "Hyperlordosis (in some patients)" [OMIM:Hyperlordosis (in some patients)]
UMLS:C0599412 "lordosis" [HPO:0003307]
UMLS:C1846834 "Hyperlordosis" [HPO:0003307]
UMLS:C0024003 "Lordosis" [Orphanet:16090]
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)
                      Hyperlordosis(HPO:0003307)
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)
          Hyperlordosis(HPO:0003307)
Database Frequency: 122 / 7739
Resource:

All diseases associated with this symptom:

3M syndrome (Orphanet:2616)
Absence deformity of leg - cataract (Orphanet:2310)
Achondroplasia (Orphanet:15)
Acrocapitofemoral dysplasia (Orphanet:63446)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Alexander disease (Orphanet:58)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal dominant congenital benign spinal muscular atrophy (Orphanet:1216)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
Autosomal recessive limb-girdle muscular dystrophy type 2O (Orphanet:206564)
Autosomal recessive lower motor neuron disease with childhood onset (Orphanet:206580)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Branchio-oculo-facial syndrome (Orphanet:1297)
CK syndrome (Orphanet:251383)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Camurati-Engelmann disease (Orphanet:1328)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Congenital bowing of long bones (Orphanet:2292)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
Corneal-cerebellar syndrome (Orphanet:3177)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
DYSTONIA WITH RINGBINDEN (OMIM:224550)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Desbuquois syndrome (Orphanet:1425)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal arthrogryposis type 5D (Orphanet:329457)
Distal spinal muscular atrophy type 3 (Orphanet:139547)
Duchenne and Becker muscular dystrophy (Orphanet:262)
Duchenne muscular dystrophy (Orphanet:98896)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Dysostosis, Stanescu type (Orphanet:1798)
Early-onset generalized limb-onset dystonia (Orphanet:256)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
Facioscapulohumeral dystrophy (Orphanet:269)
GM1 gangliosidosis (Orphanet:354)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Hallermann-Streiff syndrome (Orphanet:2108)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Humerus trochlea aplasia (Orphanet:3383)
Hypochondroplasia (Orphanet:429)
Iniencephaly (Orphanet:63259)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated glycerol kinase deficiency (Orphanet:408)
Kniest dysplasia (Orphanet:485)
Lateral meningocele syndrome (Orphanet:2789)
MASA syndrome (Orphanet:2466)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 (OMIM:615761)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYASTHENIC SYNDROME, CONGENITAL, 14 (OMIM:616228)
MYASTHENIC SYNDROME, CONGENITAL, 16 (OMIM:614198)
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET (OMIM:300718)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Microphthalmia, Lenz type (Orphanet:568)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Multiple endocrine neoplasia type 2B (Orphanet:247709)
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 (OMIM:600462)
Myotonia permanens (Orphanet:99735)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX (OMIM:162370)
Nemaline myopathy (Orphanet:607)
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa (Orphanet:2653)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pfeiffer syndrome (Orphanet:710)
Pseudoachondroplasia (Orphanet:750)
Pycnodysostosis (Orphanet:763)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SPONASTRIME dysplasia (Orphanet:93357)
Satoyoshi syndrome (Orphanet:3130)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Schwartz-Jampel syndrome (Orphanet:800)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloenchondrodysplasia (Orphanet:1855)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia (Orphanet:253)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Synaptic congenital myasthenic syndromes (Orphanet:98915)
THREE M SYNDROME 1 (OMIM:273750)
THREE M SYNDROME 2 (OMIM:612921)
THREE M SYNDROME 3 (OMIM:614205)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Thoracomelic dysplasia (Orphanet:1803)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Williams syndrome (Orphanet:904)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)
Zlotogora-Ogur syndrome (Orphanet:3253)