Hyperlordosis
Symptom Information:
Symptom ID: | HPO:0003307 | ||||||||||||||
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) 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) |
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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) |