What is Back conditions?

What is Back conditions?

Any condition that affects the back. The back is made up of numerous muscles and bones and thus there is a variety of conditions ...more »

• Back conditions: A group of conditions that affect the back.

Back conditions: Introduction

Types of Back conditions:

Types of Back conditions:

• Back pain
• Sciatica
• Disc Disorders
• Herniated disc
• Back Impairment
• Spinal conditions
• Spinal cord injury
• Osteoarthritis
• Reiter’s syndrome
• Lordosis
• Lumbago
• Spinal Cord Damage-Induced Synesthesia
• Back tumour
• Vertebral fracture
• Spinal curvature
• Adolescent idiopathic scoliosis
• Spinal stenosis
• Scoliosis
• Kyphosis
• Idiopathic adolescent scoliosis
• Spinocerebellar ataxia, autosomal recessive 6
• Spinocerebellar ataxia 18
• Spinocerebellar ataxia 27
• Spinocerebellar ataxia 19
• Spinocerebellar ataxia 28
• Spinocerebellar ataxia 29
• Spinocerebellar ataxia, autosomal dominant
• Spinocerebellar ataxia, autosomal recessive 4
• Spinocerebellar ataxia 16
• Spinocerebellar ataxia 25
• Spinocerebellar ataxia 11
• Spinocerebellar ataxia 20
• Spinocerebellar ataxia 12
• Spinocerebellar ataxia 21
• Spinocerebellar ataxia, autosomal recessive 1
• Spinocerebellar ataxia 13
• Spinocerebellar ataxia 22
• Spinocerebellar ataxia 14
• Spinocerebellar ataxia 23
• Spinocerebellar ataxia, autosomal recessive 3
• Spinocerebellar ataxia 15
• Spinocerebellar ataxia, autosomal recessive 5
• Spinocerebellar ataxia 17
• Spinocerebellar ataxia 26
• Psoriasis on lower back
• Progressive Spinobulbar muscular atrophy
• Kennedy Syndrome
• Spinal Muscular Atrophy
• Spinal Muscular Atrophy type I
• Spinal Muscular Atrophy type II
• Spinal Muscular Atrophy type III
• Adult SMA
• Adult progressive spinal muscular atrophy, Aran Duchenne type
• Spinocerebellar ataxia 2
• Spinocerebellar ataxia 4
• Spinocerebellar ataxia 5
• Spinocerebellar ataxia, Machado-Joseph type I
• Spinocerebellar ataxia, X-linked, 2
• Spinocerebellar ataxia, X-linked, 3
• Cleft palate -- short stature -- vertebral anomalies
• Opthalmoplegia progressive external scoliosis
• Proximal spinal muscular atrophy, type IV
• Spinal muscular atrophy, Adult form
• Type I spinal osteoporosis
• Seronegative spondyloarthropathy
• Spine osteoarthritis
• Spondylolisthesis
• Spinal Cord Disorders
• Spinal Cord Tumor
• Scoliosis, Idiopathic, Susceptibility to, 5
• Scoliosis, Idiopathic, Susceptibility to, 4
• Scoliosis, Idiopathic, Susceptibility to, 3
• Scoliosis, Idiopathic, Susceptibility to, 2
• Scoliosis, Idiopathic, Susceptibility to, 1
• Chronic Back pain
• Optic-spinal form of multiple sclerosis
• Lower back muscle strain
• Upper back muscle strain
• Autoimmune Myelopathy
• Spondylosis
• Spondylitis
• Ankylosing Spondylitis
• Degenerative Disc Disease
• Swayback
• Lower back sprain
• Upper back sprain
• Back sprain
• Primary osteoporosis
• Septic arthritis like stiff back
• Spinal pain and rigidity
• Ehlers-Danlos syndrome, 6B
• Ehlers-Danlos syndrome type VI
• Ehlers-Danlos syndrome type IX
• Ehlers-Danlos syndrome, kyphoscoliosis type
• Arnold-Chiari malformation type 2
• Osteogenesis imperfecta, type 3
• Osteogenesis imperfecta, type 4
• Osteogenesis imperfecta, type 5
• Osteogenesis imperfecta, type 6
• Osteogenesis imperfecta type IV
• Spinocerebellar ataxia 3
• Spinal bulbar motor neuropathy
• Proximal spinal muscular atrophy, type 3
• Spina bifida -- hypospadias
• Spinocerebellar ataxia, autosomal recessive 2
• Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
• Ophthalmoplegia, progressive external -- scoliosis
• Mental retardation -- short stature -- scoliosis
• Spinocerebellar ataxia, autosomal recessive 7
• Back injuries
• Spinocerebellar ataxia, autosomal recessive 9
• Spinocerebellar ataxia 8
• Spinocerebellar ataxia, X-linked, 5
• Spinocerebellar ataxia -- dysmorphism
• Spinocerebellar ataxia with axonal neuropathy, type 2
• Spinocerebellar ataxia, X-linked, type 4
• Spinocerebellar Ataxia 9
• Friedreich's ataxia
• Spinocerebellar Ataxia
• Progressive muscular atrophy
• Coccyx injury
• Spinal Arthritis
• Spondylarthropathy
• Friedreich ataxia
• Spinal muscular atrophy, type 3
• Spinal muscular atrophy with respiratory distress 1
• Spinal muscular atrophy type 2
• Spinal muscular atrophy, type I, with congenital bone fractures
• Spinal muscular atrophy, Ryukyuan type
• Sacroilitis
• Myelopathy
• Piriformis Syndrome
• Psoas sign
• Pilonidal disease
• Infantile onset spinocerebellar ataxia
• Scoliosis as part of NF
• Scoliosis with unilateral unsegmented bar
• Spondylarthritis
• Spinocerebellar ataxia, X-linked, 4
• Spinocerebellar ataxia, Machado-Joseph type IV
• Spinocerebellar degenerescence, book type
• Spinocerebellar ataxia, Machado-Joseph type III
• Spinocerebellar ataxia 10
• Spinocerebellar ataxia, Machado-Joseph type II
• Spinocerebellar ataxia, Machado-Joseph type V
• Spinocerebellar ataxia -- amyotrophy -- deafness
• Spinocerebellar ataxia-dysmorphism syndrome
• Oculoauriculovertebral (OAV) dysplasia
• Goldenhar Syndrome
• Proximal spinal muscular atrophy, type 4
• Proximal spinal muscular atrophy
• Congenital benign spinal muscular atrophy dominant
• Pontocerebellar hypoplasia with infantile spinal muscular atrophy
• Arthrogryposis -- spinal muscular atrophy
• Progressive spinal muscular atrophy
• Spinal muscular atrophy -- Dandy-Walker complex -- cataracts
• Spinal muscular atrophy, scapuloperoneal
• Proximal spinal muscular atrophy, type 1
• Brachydactyly -- scoliosis -- carpal fusion
• Discitis
• Pena Shokeir syndrome, type 1
• Pena-Shokeir syndrome Type 2
• COFS syndrome
• Cerebro-Oculo-Facio-Skeletal Syndrome
• Arthrogryposis, distal, type 2A
• Freeman-Sheldon Syndrome
• Whistling face syndrome
• Hydrocephalus -- costovertebral dysplasia -- Sprengel anomaly
• Hydrocephaly tall stature joint laxity and kyphoscoliosis
• Ischio-vertebral syndrome
• Ischio-spinal dysostosis
• Ischio-spinal dysostosis with cystic kidney disease
• Ischio-spinal dysostosis -- rib gaps -- nephroblastomatosis
• Spondylometaphyseal dysplasia with dentinogenesis imperfecta
• Ankylosing spondylarthritis
• Myelitis
• Transverse myelitis
• Spina bifida
• Congenital SMA with arthrogryposis
• Meningomyelocele
• Renal agenesis -- meningomyelocele -- mullerian defect
• Anencephaly and spina bifida X-linked
• Lipomyelomeningocele
• Meningocele
• Sacral meningocele -- conotruncal heart defects
• Sacral defect and anterior sacral meningocele
• Lateral meningocele syndrome
• Perineal hemangioma -- external genitalia malformations -- lipomyelomeningocele -- vesicorenal abnormalities -- imperforate anus
• Friedreich ataxia -- congenital glaucoma
• Vacuolar myopathy
• Congenital muscular dystrophy syringomyelia
• Syringomyelia
• Tethered Spinal Cord Syndrome
• Syringomyelia, cervical lesion
• Syringomyelia, lumbar lesion
• Shprintzen omphalocele syndrome
• Omphalocele -- exstrophy -- imperforate anus
• Spinal cord neoplasm
• Roussy-Levy hereditary areflexic dystasia
• Cloverleaf skull micromelia thoracic dysplasia
• Polydactyly postaxial dental and vertebral
• Ossification of the posterior longitudinal ligament of the spine
• Intervertebral disc disease
• Machado-Joseph Disease
• Brachial Plexus Injury
• Brown-Sequard Syndrome
• Intrathoracic kidney -- vertebral fusion
• Anemia, sideroblastic spinocerebellar ataxia
• Congenital stenosis of cervical medullary canal
• Spondyloepiphyseal dysplasia tarda, autosomal dominant
• Spondyloepiphyseal dysplasia tarda progressive arthropathy
• Spondyloepiphyseal dysplasia
• Spondyloepiphyseal dysplasia -- nephrotic syndrome
• Spondyloepiphyseal dysplasia tarda, Toledo type
• Spondyloepiphyseal dysplasia -- nephritic syndrome
• Oto-spondylo-megaepiphyseal dysplasia, autosomal recessive
• Oto-spondylo-megaepiphyseal dysplasia, homozygous
• Spondyloepiphyseal dysplasia tarda
• Spondyloepiphyseal dysplasia, congenita
• Otospondylomegaepiphyseal dysplasia
• Aphalangy -- hemivertebrae -- urogenital-intestinal dysgenesis
• Kahrizi Syndrome
• Spondyloepimetaphyseal Dysplasia, Aggrecan Type
• Spondylodysplasia and Premature Pubarche
• Spondyloepimetaphyseal Dysplasia, Pakistani Type
• Spinal AVM
• Metaphyseal undermodeling, spondylar dysplasia, and overgrowth
• Ischio-vertebral dysplasia
• Multiple vertebral anomalies unusual facies
• Scheuermann juvenile Kyphosis, familial
• Mirror polydactyly -- vertebral segmentation -- limbs defects
• Spinal shock
• Segmental vertebral anomalies
• Polydactyly, postaxial -- dental and vertebral anomalies
• Microsomia -- hemifacial -- radial defects
• Spondylocostal dysostosis with anal atresia and urogenital anomalies
• Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction
• Cleft lip palate -- deafness -- sacral lipoma
• Dysraphism -- cleft lip palate -- limb reduction defects
• Leg absence -- deformity -- cataract
• Caudal dysplasia sequence
• Caudal regression syndrome
• Holoprosencephaly -- caudal dysgenesis
• Caudal appendage -- deafness
• Caudal duplication
• Spondylocarpotarsal synostosis
• Diaphanospondylodysostosis
• Spondylohypoplasia arthrogryposis popliteal pterygium
• Goodman camptodactyly
• Spondylo camptodactyly syndrome
• Tel-Hashomer camptodactyly syndrome
• Syncamptodactyly -- scoliosis
• Camptodactyly -- vertebral fusion
• VATER association
• Spondyloepimetaphyseal dysplasia, hypotrichosis
• Spondylometaphyseal dysplasia -- cone-rod dystrophy
• Spondylometaphyseal dysplasia, axial
• Spondylometaphyseal dysplasia, Algerian type
• Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
• Spondylometaphyseal dysplasia, east-African type
• Spondylometaphyseal dysplasia, Sedaghatian type
• Spondylometaphyseal dysplasia, 'corner fracture' type
• Spondylometaphyseal dysplasia, Kozlowski type
• Spondylometaphyseal dysplasia with combined immunodeficiency
• Spondylometaphyseal dysplasia, X-linked
• VACTERL with hydrocephalus, X-linked
• VACTERL association
• VACTERYL hydrocephaly
• VACTERL association with hydrocephaly, X-linked
• Thanatophoric dysplasia, type 2
• Thanatophoric dysplasia, type 1
• Spinal intradural arachnoid cysts
• Spinal atrophy -- ophthalmoplegia -- pyramidal syndrome
• Spondylocostal dysostosis, autosomal recessive 3
• Spondylocostal dysostosis, autosomal recessive 1
• Spondylocostal dysostosis, autosomal recessive 2
• Spinal dysostosis, type Anhalt
• Spondylohypoplasia, arthrogryposis and popliteal pterygium
• Skeletal dysplasia, San Diego type
• Spondyloepimetaphyseal dysplasia with joint laxity
• Spondylocostal dysostosis, autosomal recessive
• Spondylocostal dysplasia dominant
• Spondyloepimetaphyseal dysplasia, micromelic
• Spondyloepimetaphyseal dysplasia congenita, Iraqi
• Platyspondylic lethal chondrodysplasia
• Platyspondylic lethal skeletal dysplasia, Torrance type
• Acrodysplasia scoliosis
• Acropectorovertebral dysplasia
• Alves Castelo dos Santos syndrome
• Spondylo-humero-femoral dysplasia
• Microcephaly brachydactyly kyphoscoliosis
• Anterior spinal artery stroke
• Anterior cord syndrome
• Anterior spinal artery syndrome
• Dysspondyloenchondromatosis
• Syringomelia
• Lumbar malsegmentation, short stature and facial anomalies
• Scheuermann's disease
• Vertebral body fusion overgrowth
• Vertebral fusion posterior lumbosacral blepharoptosis
• Cauda equina syndrome
• Spondylo-ocular syndrome
• Spondyloenchondrodysplasia
• Facet syndrome
• Cutaneomeningospinal angiomatosis
• Scapulocostal syndrome
• Schanz disease
• Schanz's syndrome
• Seven point syndrome
• Spondyloepimetaphyseal dysplasia, genevieve type
• Whistling face syndrome, recessive form
• Putti-Chavany syndrome
• Escobar syndrome, type B
• Fryns-Fabry-Remans syndrome
• Johnson-Munson syndrome
• Breakdance back syndrome
• Bruns-Garland syndrome
• Dreyfus syndrome
• Foix-Alajouanine syndrome
• Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
• Michels-Caskey syndrome
• Diastematomyelia
• Melhem-Fahl syndrome
• Nathalie syndrome
• Spondylocostal dysostosis, Dandy-Walker
• Sacral hemangiomas -- multiple congenital abnormalities
• Spondyloepimetaphyseal dysplasia, X linked with mental deterioration
• Spondyloepimetaphyseal dysplasia, Missouri type
• Spondyloepimetaphyseal dysplasia with multiple dislocations
• Diphallus -- rachischisis -- imperforate anus
• Spondyloepimetaphyseal dysplasia, X-linked
• Spondyloepimetaphyseal dysplasia, Irapa type
• Spondyloperipheral dysplasia -- short ulna
• Spondyloepimetaphyseal dysplasia joint laxity
• Sacrococcygeal dysgenesis association
• McDonough syndrome
• Seghers syndrome
• Vertebral fusion- posterior lumbrosacral, blepharoptosis
• Spondyloepimetaphyseal dysplasia with hypotrichosis
• Tsukuhara syndrome
• Notalgia paresthetica
• Tarlov cysts
• Brachyrachia
• Beardwell syndrome
• Sacral agenesis
• Saul-Wilkes-Stevenson syndrome
• Boucher-Neuhauser syndrome
• Currarino triad
• Barre-Lieou syndrome
• Fazio-Londe syndrome
• Occult spinal dysraphism
• Jeune syndrome
• more types...»

Broader types of Back conditions:

• All Disease Categories
• more types...»

What causes Back conditions?

Causes of Back conditions: see causes of Back conditions

What are the symptoms of Back conditions?

Symptoms of Back conditions: see symptoms of Back conditions

How is it treated?

Doctors and Medical Specialists for Back conditions: Neurologist, Orthopedic Surgeon ; see also doctors and medical specialists for Back conditions.
Treatments for Back conditions: see treatments for Back conditions
Research for Back conditions: see research for Back conditions

Organs Affected by Back conditions:

Organs and body systems related to Back conditions include:

• Back

Name and Aliases of Back conditions

Main name of condition: Back conditions

Back disorders, Back problems

Back conditions: Related Conditions

Research the causes of these diseases that are similar to, or related to, Back conditions:

• Anklosing spondylitis
• Tuberculosis
• Cold abscess
• Sciatica
• Spina bifida
• Disc prolapsed
• Lumbago
• Osteoporosis
• Spinal infarct

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