List of MeSH codes (C05)
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).
This list continues the information at List of MeSH codes (C04). Codes following these are found at List of MeSH codes (C06). For other MeSH codes, see List of MeSH codes.
The source for this content is the set of 2006 MeSH Trees from the NLM.
MeSH C05 – musculoskeletal diseases
MeSH C05.116.070 – bone cysts
- MeSH C05.116.070.265 – bone cysts, aneurysmal
MeSH C05.116.099 – bone diseases, developmental
- MeSH C05.116.099.052 – acro-osteolysis
- MeSH C05.116.099.052.400 – Hajdu–Cheney syndrome
- MeSH C05.116.099.105 – basal-cell nevus syndrome
- MeSH C05.116.099.343 – dwarfism
- MeSH C05.116.099.343.110 – achondroplasia
- MeSH C05.116.099.343.250 – cockayne syndrome
- MeSH C05.116.099.343.347 – congenital hypothyroidism
- MeSH C05.116.099.343.445 – dwarfism, pituitary
- MeSH C05.116.099.343.679 – Laron syndrome
- MeSH C05.116.099.343.796 – Mulibrey nanism
- MeSH C05.116.099.343.914 – thanatophoric dysplasia
- MeSH C05.116.099.370 – dysostoses
- MeSH C05.116.099.370.231 – craniofacial dysostosis
- MeSH C05.116.099.370.231.427 – Hallermann's syndrome
- MeSH C05.116.099.370.231.480 – hypertelorism
- MeSH C05.116.099.370.231.576 – mandibulofacial dysostosis
- MeSH C05.116.099.370.231.576.410 – goldenhar syndrome
- MeSH C05.116.099.370.380 – focal dermal hypoplasia
- MeSH C05.116.099.370.535 – Klippel–Feil syndrome
- MeSH C05.116.099.370.652 – orofaciodigital syndromes
- MeSH C05.116.099.370.797 – Rubinstein–Taybi syndrome
- MeSH C05.116.099.370.894 – synostosis
- MeSH C05.116.099.370.894.232 – craniosynostoses
- MeSH C05.116.099.370.894.232.015 – acrocephalosyndactylia
- MeSH C05.116.099.370.894.819 – syndactyly
- MeSH C05.116.099.370.894.819.100 – acrocephalosyndactylia
- MeSH C05.116.099.370.894.819.756 – Poland syndrome
- MeSH C05.116.099.386 – funnel chest
- MeSH C05.116.099.492 – gigantism
- MeSH C05.116.099.655 – leg length inequality
- MeSH C05.116.099.674 – Marfan syndrome
- MeSH C05.116.099.708 – osteochondrodysplasias
- MeSH C05.116.099.708.017 – achondroplasia
- MeSH C05.116.099.708.195 – chondrodysplasia punctata
- MeSH C05.116.099.708.195.200 – chondrodysplasia punctata, rhizomelic
- MeSH C05.116.099.708.207 – cleidocranial dysplasia
- MeSH C05.116.099.708.281 – diaphyseal dysplasia, progressive
- MeSH C05.116.099.708.327 – Ellis–van Creveld syndrome
- MeSH C05.116.099.708.338 – enchondromatosis
- MeSH C05.116.099.708.375 – fibrous dysplasia of bone
- MeSH C05.116.099.708.375.199 – cherubism
- MeSH C05.116.099.708.375.372 – fibrous dysplasia, monostotic
- MeSH C05.116.099.708.375.381 – fibrous dysplasia, polyostotic
- MeSH C05.116.099.708.479 – hyperostosis, cortical, congenital
- MeSH C05.116.099.708.486 – hyperostosis frontalis interna
- MeSH C05.116.099.708.582 – Langer–Giedion syndrome
- MeSH C05.116.099.708.670 – osteochondroma
- MeSH C05.116.099.708.670.615 – osteochondromatosis
- MeSH C05.116.099.708.670.615.325 – exostoses, multiple hereditary
- MeSH C05.116.099.708.685 – osteogenesis imperfecta
- MeSH C05.116.099.708.702 – osteosclerosis
- MeSH C05.116.099.708.702.593 – melorheostosis
- MeSH C05.116.099.708.702.678 – osteopetrosis
- MeSH C05.116.099.708.702.685 – osteopoikilosis
- MeSH C05.116.099.708.800 – acquired hyperostosis syndrome
- MeSH C05.116.099.708.857 – short rib–polydactyly syndrome
- MeSH C05.116.099.708.914 – thanatophoric dysplasia
- MeSH C05.116.099.736 – osteolysis, essential
- MeSH C05.116.099.742 – platybasia
- MeSH C05.116.099.750 – Proteus syndrome
MeSH C05.116.132 – bone diseases, endocrine
- MeSH C05.116.132.082 – acromegaly
- MeSH C05.116.132.256 – congenital hypothyroidism
- MeSH C05.116.132.358 – dwarfism, pituitary
- MeSH C05.116.132.479 – gigantism
- MeSH C05.116.132.684 – osteitis fibrosa cystica
MeSH C05.116.165 – bone diseases, infectious
- MeSH C05.116.165.412 – osteitis
- MeSH C05.116.165.495 – osteomyelitis
- MeSH C05.116.165.595 – periostitis
- MeSH C05.116.165.762 – spondylitis
- MeSH C05.116.165.762.301 – discitis
- MeSH C05.116.165.886 – tuberculosis, osteoarticular
- MeSH C05.116.165.886.722 – tuberculosis, spinal
MeSH C05.116.198 – bone diseases, metabolic
- MeSH C05.116.198.247 – bone demineralization, pathologic
- MeSH C05.116.198.247.400 – decalcification, pathologic
- MeSH C05.116.198.371 – mucolipidoses
- MeSH C05.116.198.495 – osteomalacia
- MeSH C05.116.198.579 – osteoporosis
- MeSH C05.116.198.579.610 – osteoporosis, postmenopausal
- MeSH C05.116.198.709 – pseudohypoparathyroidism
- MeSH C05.116.198.709.628 – pseudopseudohypoparathyroidism
- MeSH C05.116.198.762 – renal osteodystrophy
- MeSH C05.116.198.816 – rickets
MeSH C05.116.214 – bone malalignment
MeSH C05.116.231 – bone neoplasms
- MeSH C05.116.231.030 – adamantinoma
- MeSH C05.116.231.343 – femoral neoplasms
- MeSH C05.116.231.754 – skull neoplasms
- MeSH C05.116.231.754.450 – jaw neoplasms
- MeSH C05.116.231.754.450.583 – mandibular neoplasms
- MeSH C05.116.231.754.450.601 – maxillary neoplasms
- MeSH C05.116.231.754.450.692 – palatal neoplasms
- MeSH C05.116.231.754.600 – nose neoplasms
- MeSH C05.116.231.754.659 – orbital neoplasms
- MeSH C05.116.231.754.829 – skull base neoplasms
- MeSH C05.116.231.828 – spinal neoplasms
MeSH C05.116.264 – bone resorption
- MeSH C05.116.264.143 – ainhum
- MeSH C05.116.264.150 – alveolar bone loss
- MeSH C05.116.264.579 – osteolysis
- MeSH C05.116.264.579.052 – acro-osteolysis
- MeSH C05.116.264.579.052.400 – Hajdu–Cheney syndrome
- MeSH C05.116.264.579.704 – osteolysis, essential
MeSH C05.116.425 – epiphyses, slipped
MeSH C05.116.540 – hyperostosis
- MeSH C05.116.540.310 – exostoses
- MeSH C05.116.540.310.500 – exostoses, multiple hereditary
- MeSH C05.116.540.310.600 – heel spur
- MeSH C05.116.540.400 – hyperostosis, cortical, congenital
- MeSH C05.116.540.410 – hyperostosis, diffuse idiopathic skeletal
- MeSH C05.116.540.420 – hyperostosis frontalis interna
- MeSH C05.116.540.600 – hyperostosis, sternocostoclavicular
MeSH C05.116.692 – osteitis deformans
MeSH C05.116.725 – osteoarthropathy, primary hypertrophic
MeSH C05.116.758 – osteoarthropathy, secondary hypertrophic
MeSH C05.116.852 – osteonecrosis
- MeSH C05.116.852.175 – femur head necrosis
- MeSH C05.116.852.175.570 – Legg–Perthes disease
MeSH C05.116.900 – spinal diseases
- MeSH C05.116.900.307 – intervertebral disc displacement
- MeSH C05.116.900.480 – ossification of posterior longitudinal ligament
- MeSH C05.116.900.540 – platybasia
- MeSH C05.116.900.653 – scheuermann's disease
- MeSH C05.116.900.800 – spinal curvatures
- MeSH C05.116.900.800.500 – kyphosis
- MeSH C05.116.900.800.750 – lordosis
- MeSH C05.116.900.800.875 – scoliosis
- MeSH C05.116.900.801 – spinal neoplasms
- MeSH C05.116.900.802 – spinal osteophytosis
- MeSH C05.116.900.802.651 – hyperostosis, diffuse idiopathic skeletal
- MeSH C05.116.900.805 – spinal stenosis
- MeSH C05.116.900.845 – spondylarthritis
- MeSH C05.116.900.845.800 – spondylarthropathies
- MeSH C05.116.900.845.800.145 – arthritis, psoriatic
- MeSH C05.116.900.853.625.800.637 – reactive arthritis
- MeSH C05.116.900.845.800.850 – spondylitis, ankylosing
- MeSH C05.116.900.853 – spondylitis
- MeSH C05.116.900.853.500 – discitis
- MeSH C05.116.900.853.750 – spondylitis, ankylosing
- MeSH C05.116.900.853.850 – tuberculosis, spinal
- MeSH C05.116.900.877 – spondylolisthesis
- MeSH C05.116.900.877.500 – spondylolysis
MeSH C05.182.531 – polychondritis, relapsing
MeSH C05.321.550 – fasciitis, necrotizing
MeSH C05.321.600 – fasciitis, plantar
MeSH C05.330.488 – foot deformities, acquired
- MeSH C05.330.488.099 – bunion, tailor's
- MeSH C05.330.488.200 – equinus deformity
- MeSH C05.330.488.300 – hallux limitus
- MeSH C05.330.488.310 – hallux rigidus
MeSH C05.330.495 – foot deformities, congenital
MeSH C05.330.610 – hallux valgus
MeSH C05.330.615 – hammer toe syndrome
MeSH C05.360.350 – fasciitis, plantar
MeSH C05.360.400 – heel spur
MeSH C05.360.750 – posterior tibial tendon dysfunction
MeSH C05.390.110 – hand deformities, acquired
MeSH C05.390.408 – hand deformities, congenital
MeSH C05.500.368 – granuloma, giant cell
MeSH C05.500.460 – jaw abnormalities
- MeSH C05.500.460.185 – cleft palate
- MeSH C05.500.460.457 – micrognathism
- MeSH C05.500.460.606 – Pierre Robin syndrome
- MeSH C05.500.460.655 – prognathism
- MeSH C05.500.460.813 – retrognathism
MeSH C05.500.470 – jaw cysts
- MeSH C05.500.470.660 – nonodontogenic cysts
- MeSH C05.500.470.690 – odontogenic cysts
- MeSH C05.500.470.690.150 – basal cell nevus syndrome
- MeSH C05.500.470.690.310 – dentigerous cyst
- MeSH C05.500.470.690.605 – odontogenic cyst, calcifying
- MeSH C05.500.470.690.790 – periodontal cyst
- MeSH C05.500.470.690.790.820 – radicular cyst
MeSH C05.500.480 – jaw, edentulous
- MeSH C05.500.480.450 – jaw, edentulous, partially
MeSH C05.500.499 – jaw neoplasms
- MeSH C05.500.499.583 – mandibular neoplasms
- MeSH C05.500.499.601 – maxillary neoplasms
- MeSH C05.500.499.692 – palatal neoplasms
MeSH C05.500.607 – mandibular diseases
- MeSH C05.500.607.221 – craniomandibular disorders
- MeSH C05.500.607.221.897 – temporomandibular joint disorders
- MeSH C05.500.607.221.897.897 – temporomandibular joint dysfunction syndrome
- MeSH C05.500.607.442 – mandibular neoplasms
- MeSH C05.500.607.655 – prognathism
- MeSH C05.500.607.813 – retrognathism
MeSH C05.500.693 – maxillary diseases
- MeSH C05.500.693.528 – maxillary neoplasms
MeSH C05.550.069 – ankylosis
- MeSH C05.550.069.680 – spondylitis, ankylosing
MeSH C05.550.091 – arthralgia
- MeSH C05.550.091.700 – shoulder pain
MeSH C05.550.114 – arthritis
- MeSH C05.550.114.015 – arthritis, experimental
- MeSH C05.550.114.099 – arthritis, infectious
- MeSH C05.550.114.099.500 – arthritis, reactive
- MeSH C05.550.114.145 – arthritis, psoriatic
- MeSH C05.550.114.154 – arthritis, rheumatoid
- MeSH C05.550.114.154.114 – arthritis, juvenile rheumatoid
- MeSH C05.550.114.154.219 – Caplan's syndrome
- MeSH C05.550.114.154.389 – Felty's syndrome
- MeSH C05.550.114.154.683 – rheumatoid nodule
- MeSH C05.550.114.154.774 – Sjögren syndrome
- MeSH C05.550.114.154.856 – spondylitis, ankylosing
- MeSH C05.550.114.154.870 – Still's disease, adult-onset
- MeSH C05.550.114.264 – chondrocalcinosis
- MeSH C05.550.114.423 – gout
- MeSH C05.550.114.423.410 – arthritis, gouty
- MeSH C05.550.114.606 – osteoarthritis
- MeSH C05.550.114.606.400 – osteoarthritis, hip
- MeSH C05.550.114.606.500 – osteoarthritis, knee
- MeSH C05.550.114.606.761 – spinal osteophytosis
- MeSH C05.550.114.678 – periarthritis
- MeSH C05.550.114.865.800.637 – reactive arthritis
- MeSH C05.550.114.843 – rheumatic fever
- MeSH C05.550.114.843.566 – rheumatic nodule
- MeSH C05.550.114.843.823 – Wissler's syndrome
- MeSH C05.550.114.865 – spondylarthritis
- MeSH C05.550.114.865.800 – spondylarthropathies
- MeSH C05.550.114.865.800.145 – arthritis, psoriatic
- MeSH C05.550.114.865.800.150 – arthritis, reactive
- MeSH C05.550.114.865.800.782 – Reiter disease
- MeSH C05.550.114.865.800.850 – spondylitis, ankylosing
MeSH C05.550.186 – arthropathy, neurogenic
MeSH C05.550.251 – bursitis
- MeSH C05.550.251.595 – periarthritis
MeSH C05.550.287 – chondromatosis, synovial
MeSH C05.550.323 – contracture
- MeSH C05.550.323.468 – hip contracture
MeSH C05.550.445 – hallux limitus
MeSH C05.550.485 – hip dislocation, congenital
MeSH C05.550.509 – hydrarthrosis
MeSH C05.550.515 – joint deformities, acquired
MeSH C05.550.521 – joint instability
MeSH C05.550.535 – joint loose bodies
MeSH C05.550.629 – nail-patella syndrome
MeSH C05.550.648 – osteoarthropathy, primary hypertrophic
MeSH C05.550.684 – osteoarthropathy, secondary hypertrophic
MeSH C05.550.870 – synovitis
- MeSH C05.550.870.890 – synovitis, pigmented villonodular
MeSH C05.550.905 – temporomandibular joint disorders
- MeSH C05.550.905.905 – temporomandibular joint dysfunction syndrome
MeSH C05.651.180 – compartment syndromes
MeSH C05.651.197 – contracture
- MeSH C05.651.197.270 – Dupuytren's contracture
- MeSH C05.651.197.468 – hip contracture
MeSH C05.651.243 – craniomandibular disorders
- MeSH C05.651.243.897 – temporomandibular joint disorders
- MeSH C05.651.243.897.897 – temporomandibular joint dysfunction syndrome
MeSH C05.651.290 – eosinophilia-myalgia syndrome
MeSH C05.651.310 – fatigue syndrome, chronic
MeSH C05.651.392 – Isaacs syndrome
MeSH C05.651.460 – mitochondrial myopathies
- MeSH C05.651.460.620 – mitochondrial encephalomyopathies
- MeSH C05.651.460.620.520 – MELAS syndrome
- MeSH C05.651.460.620.530 – MERRF syndrome
- MeSH C05.651.460.700 – ophthalmoplegia, chronic progressive external
- MeSH C05.651.460.700.500 – Kearns–Sayre syndrome
MeSH C05.651.475 – muscle cramp
MeSH C05.651.494 – muscle neoplasms
MeSH C05.651.504 – muscle rigidity
MeSH C05.651.512 – muscle spasticity
MeSH C05.651.534 – muscular disorders, atrophic
- MeSH C05.651.534.500 – muscular dystrophies
- MeSH C05.651.534.500.074 – distal myopathies
- MeSH C05.651.534.500.149 – glycogen storage disease type vii
- MeSH C05.651.534.500.280 – muscular dystrophies, limb-girdle
- MeSH C05.651.534.500.300 – muscular dystrophy, duchenne
- MeSH C05.651.534.500.350 – muscular dystrophy, emery-dreifuss
- MeSH C05.651.534.500.400 – muscular dystrophy, facioscapulohumeral
- MeSH C05.651.534.500.450 – muscular dystrophy, oculopharyngeal
- MeSH C05.651.534.500.500 – myotonic dystrophy
- MeSH C05.651.534.750 – postpoliomyelitis syndrome
MeSH C05.651.550 – myofascial pain syndromes
- MeSH C05.651.550.905 – temporomandibular joint dysfunction syndrome
MeSH C05.651.575 – myopathies, structural, congenital
- MeSH C05.651.575.290 – myopathies, nemaline
- MeSH C05.651.575.300 – myopathy, central core
MeSH C05.651.594 – myositis
- MeSH C05.651.594.297 – dermatomyositis
- MeSH C05.651.594.600 – myositis, inclusion body
- MeSH C05.651.594.638 – myositis ossificans
- MeSH C05.651.594.819 – polymyositis
- MeSH C05.651.594.819.500 – dermatomyositis
MeSH C05.651.662 – myotonic disorders
MeSH C05.651.701 – paralyses, familial periodic
- MeSH C05.651.701.450 – hypokalemic periodic paralysis
- MeSH C05.651.701.600 – paralysis, hyperkalemic periodic
MeSH C05.660.207 – craniofacial abnormalities
- MeSH C05.660.207.207 – cleidocranial dysplasia
- MeSH C05.660.207.231 – craniofacial dysostosis
- MeSH C05.660.207.231.427 – Hallermann's syndrome
- MeSH C05.660.207.231.480 – hypertelorism
- MeSH C05.660.207.231.576 – mandibulofacial dysostosis
- MeSH C05.660.207.231.576.410 – Goldenhar syndrome
- MeSH C05.660.207.240 – craniosynostoses
- MeSH C05.660.207.240.100 – acrocephalosyndactylia
- MeSH C05.660.207.410 – holoprosencephaly
- MeSH C05.660.207.525 – leopard syndrome
- MeSH C05.660.207.540 – maxillofacial abnormalities
- MeSH C05.660.207.540.460 – jaw abnormalities
- MeSH C05.660.207.540.460.185 – cleft palate
- MeSH C05.660.207.540.460.457 – micrognathism
- MeSH C05.660.207.540.460.606 – Pierre Robin syndrome
- MeSH C05.660.207.540.460.655 – prognathism
- MeSH C05.660.207.540.460.813 – retrognathism
- MeSH C05.660.207.620 – microcephaly
- MeSH C05.660.207.690 – Noonan syndrome
- MeSH C05.660.207.700 – orofaciodigital syndromes
- MeSH C05.660.207.715 – plagiocephaly, nonsynostotic
- MeSH C05.660.207.720 – platybasia
- MeSH C05.660.207.850 – Rubinstein–Taybi syndrome
MeSH C05.660.386 – funnel chest
MeSH C05.660.449 – hip dislocation, congenital
MeSH C05.660.585 – limb deformities, congenital
- MeSH C05.660.585.350 – ectromelia
- MeSH C05.660.585.512 – lower extremity deformities, congenital
- MeSH C05.660.585.512.380 – foot deformities, congenital
- MeSH C05.660.585.600 – polydactyly
- MeSH C05.660.585.600.750 – short rib-polydactyly syndrome
- MeSH C05.660.585.620 – proteus syndrome
- MeSH C05.660.585.800 – syndactyly
- MeSH C05.660.585.800.100 – acrocephalosyndactylia
- MeSH C05.660.585.800.756 – poland syndrome
- MeSH C05.660.585.984 – thanatophoric dysplasia
- MeSH C05.660.585.988 – upper extremity deformities, congenital
- MeSH C05.660.585.988.425 – hand deformities, congenital
MeSH C05.799.114 – arthritis, rheumatoid
- MeSH C05.799.114.114 – arthritis, juvenile rheumatoid
- MeSH C05.799.114.219 – Caplan's syndrome
- MeSH C05.799.114.389 – Felty's syndrome
- MeSH C05.799.114.683 – rheumatoid nodule
- MeSH C05.799.114.774 – Sjögren syndrome
- MeSH C05.799.114.856 – spondylitis, ankylosing
- MeSH C05.799.114.870 – Still's disease, adult-onset
MeSH C05.799.414 – gout
- MeSH C05.799.414.410 – arthritis, gouty
MeSH C05.799.440 – hyperostosis, sternocostoclavicular
MeSH C05.799.613 – osteoarthritis
- MeSH C05.799.613.400 – osteoarthritis, hip
- MeSH C05.799.613.500 – osteoarthritis, knee
- MeSH C05.799.613.678 – spinal osteophytosis
MeSH C05.799.825 – rheumatic fever
- MeSH C05.799.825.566 – rheumatic nodule
- MeSH C05.799.825.823 – Wissler's syndrome
gollark: Do you plan to have other people make plugins ever?
gollark: <@738361430763372703> reject plugin systemreturn to recompiling code on changes
gollark: You should make a font which displays it as incomprehensible runes instead.
gollark: How is that even done, ligature abuse?
gollark: No. This is much worse oh bee oh bee.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.