7.087
7.053
6.4
5.8
5.333
7.3
8.565
6.1
5.082
6.627
6.4
5.188
5.7
7
6.2
List of MeSH codes (C05) GudangMovies21 Rebahinxxi LK21
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 – bone 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 C05.116.391 – eosinophilic granuloma
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 C05.116.680 – osteitis
MeSH C05.116.692 – osteitis deformans
MeSH C05.116.725 – osteoarthropathy, primary hypertrophic
MeSH C05.116.758 – osteoarthropathy, secondary hypertrophic
MeSH C05.116.791 – osteochondritis
MeSH C05.116.791.668 – osteochondritis dissecans
MeSH C05.116.791.835 – scheuermann's disease
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 – cartilage diseases
=
MeSH C05.182.100 – chondromalacia patellae
MeSH C05.182.520 – osteochondritis
MeSH C05.182.531 – polychondritis, relapsing
MeSH C05.182.790 – Tietze syndrome
= MeSH C05.321 – fasciitis
=
MeSH C05.321.550 – fasciitis, necrotizing
MeSH C05.321.600 – fasciitis, plantar
= MeSH C05.330 – foot deformities
=
MeSH C05.330.448 – flatfoot
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 C05.330.495.150 – clubfoot
MeSH C05.330.610 – hallux valgus
MeSH C05.330.612 – hallux varus
MeSH C05.330.615 – hammer toe syndrome
= MeSH C05.360 – foot diseases
=
MeSH C05.360.350 – fasciitis, plantar
MeSH C05.360.400 – heel spur
MeSH C05.360.500 – metatarsalgia
MeSH C05.360.750 – posterior tibial tendon dysfunction
= MeSH C05.390 – hand deformities
=
MeSH C05.390.110 – hand deformities, acquired
MeSH C05.390.408 – hand deformities, congenital
= MeSH C05.500 – jaw diseases
=
MeSH C05.500.174 – cherubism
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 – joint diseases
=
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 C05.550.150 – arthrogryposis
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 C05.550.450 – hallux rigidus
MeSH C05.550.459 – hemarthrosis
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 C05.550.610 – metatarsalgia
MeSH C05.550.629 – nail-patella syndrome
MeSH C05.550.648 – osteoarthropathy, primary hypertrophic
MeSH C05.550.684 – osteoarthropathy, secondary hypertrophic
MeSH C05.550.700 – patellofemoral pain syndrome
MeSH C05.550.840 – shoulder impingement syndrome
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 – muscular diseases
=
MeSH C05.651.102 – arthrogryposis
MeSH C05.651.180 – compartment syndromes
MeSH C05.651.180.063 – anterior compartment syndrome
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 C05.651.324 – fibromyalgia
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 C05.651.515 – muscle weakness
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 C05.651.662.500 – myotonia congenita
MeSH C05.651.662.750 – myotonic dystrophy
MeSH C05.651.701 – paralyses, familial periodic
MeSH C05.651.701.450 – hypokalemic periodic paralysis
MeSH C05.651.701.600 – paralysis, hyperkalemic periodic
MeSH C05.651.742 – polymyalgia rheumatica
MeSH C05.651.807 – rhabdomyolysis
MeSH C05.651.807.628 – myoglobinuria
MeSH C05.651.869 – tendinopathy
MeSH C05.651.869.870 – tenosynovitis
= MeSH C05.660 – musculoskeletal abnormalities
=
MeSH C05.660.077 – arthrogryposis
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 C05.660.417 – gastroschisis
MeSH C05.660.449 – hip dislocation, congenital
MeSH C05.660.551 – Klippel–Feil syndrome
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 C05.660.906 – synostosis
MeSH C05.660.906.364 – craniosynostoses
MeSH C05.660.906.364.100 – acrocephalosyndactylia
MeSH C05.660.906.819 – syndactyly
MeSH C05.660.906.819.100 – acrocephalosyndactylia
MeSH C05.660.906.819.756 – poland syndrome
= MeSH C05.799 – rheumatic diseases
=
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 C05.799.321 – fibromyalgia
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 C05.799.720 – polymyalgia rheumatica
MeSH C05.799.825 – rheumatic fever
MeSH C05.799.825.566 – rheumatic nodule
MeSH C05.799.825.823 – Wissler's syndrome
= MeSH C05.906 – tennis elbow
=
The list continues at List of MeSH codes (C06).
Kata Kunci Pencarian:
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