Muscular Diseases [nemoci svalů]

topical
557
Terms

choroby svalů
myopatie
onemocnění svalů
svaly - nemoci

 

Muscle Disorders
Myopathic Conditions
Myopathies

Persistent link   https://www.medvik.cz/link/D009135
Definition

Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.

Annotation
general or unspecified; prefer specifics; inflammatory disease equals MYOSITIS; /congen: consider also Myopathies, Structural, Congenital & its indentions
obecné, dej přednost přesnějšímu deskriptoru; zánětlivá nemoc = MYOZITIDA; podheslo /vrozené: zvaž také deskriptor MYOPATIE STRUKTURÁLNÍ VROZENÉ a podřazené deskriptory
DUI
D009135 MeSH Browser
CUI
M0014252

Allowable subheadings

BL
blood 8
CF
cerebrospinal fluid
CI
chemically induced 64
CL
classification 26
CO
complications 40
CN
congenital 6
DI
diagnosis 169
DG
diagnostic imaging 2
DH
diet therapy
DT
drug therapy 31
EC
economics
EM
embryology
EN
enzymology 2
EP
epidemiology 11
EH
ethnology
ET
etiology 136
GE
genetics 26
HI
history
IM
immunology 4
ME
metabolism 18
MI
microbiology 1
MO
mortality
NU
nursing 2
PS
parasitology 1
PA
pathology 54
PP
physiopathology 48
PC
prevention & control 16
PX
psychology
RT
radiotherapy
RH
rehabilitation 22
SU
surgery 18
TH
therapy 72
UR
urine 1
VE
veterinary 4
VI
virology

C Diseases
C05 Musculoskeletal Diseases 1 125
C05.116 Bone Diseases 796
C05.182 Cartilage Diseases 141
C05.321 Fasciitis 41
C05.330 Foot Deformities 144
C05.360 Foot Diseases 209
C05.390 Hand Deformities 51
C05.500 Jaw Diseases 134
C05.550 Joint Diseases 1 254
C05.651 Muscular Diseases 557
C05.651.102 Arthrogryposis 31
C05.651.180 Compartment Syndromes 114
C05.651.197 Contracture 154
C05.651.243 Craniomandibular Disorders 9
C05.651.290 Eosinophilia-Myalgia Syndrome 3
C05.651.310 Fatigue Syndrome, Chronic 276
C05.651.324 Fibromyalgia 134
C05.651.392 Isaacs Syndrome 7
C05.651.426 Medial Tibial Stress Syndrome 2
C05.651.460 Mitochondrial Myopathies 40
C05.651.475 Muscle Cramp 176
C05.651.494 Muscle Neoplasms 17
C05.651.504 Muscle Rigidity 47
C05.651.512 Muscle Spasticity 462
C05.651.515 Muscle Weakness 225
C05.651.534 Muscular Disorders, Atrophic 45
C05.651.538 Musculoskeletal Pain 149
C05.651.542 Myalgia 54
C05.651.550 Myofascial Pain Syndromes 92
C05.651.575 Myopathies, Structural, Congenital 15
C05.651.594 Myositis 253
C05.651.662 Myotonic Disorders 23
C05.651.682 Myotoxicity 1
C05.651.701 Paralyses, Familial Periodic 7
C05.651.742 Polymyalgia Rheumatica 111
C05.651.807 Rhabdomyolysis 128
C05.651.869 Tendinopathy 90
C05.660 Musculoskeletal Abnormalities 107
C05.799 Rheumatic Diseases 2 184
C10 Nervous System Diseases 1 884
C10.668 Neuromuscular Diseases 333
C10.668.364 Fatigue Syndrome, Chronic 276
C10.668.416 Locked-In Syndrome 3
C10.668.467 Motor Neuron Disease 63
C10.668.491 Muscular Diseases 557
C10.668.491.050 Eosinophilia-Myalgia Syndrome 3
C10.668.491.087 Medial Tibial Stress Syndrome 2
C10.668.491.175 Muscular Disorders, Atrophic 45
C10.668.491.425 Fibromyalgia 134
C10.668.491.500 Mitochondrial Myopathies 40
C10.668.491.525 Myalgia 54
C10.668.491.550 Myopathies, Structural, Congenital 15
C10.668.491.562 Myositis 253
C10.668.491.606 Myotonic Disorders 23
C10.668.491.628 Myotoxicity 1
C10.668.491.650 Paralyses, Familial Periodic 7
C10.668.758 Neuromuscular Junction Diseases 50
C10.668.829 Peripheral Nervous System Diseases 495
C10.668.864 Poliomyelitis 476
C10.668.900 Stiff-Person Syndrome 14

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Erythrocyte Lactate Transporter Defect Disease MeSH Browser

Fingerprint Body Myopathy Disease MeSH Browser

Hereditary Myopathy with Early Respiratory Failure Disease MeSH Browser

Hypertrophia Musculorum Vera Disease MeSH Browser

Kocher-Debre-Semelaigne syndrome Disease MeSH Browser

Marinesco-Sjogren-like syndrome (MSLS) Disease MeSH Browser

Mitochondrial DNA Depletion Syndrome, Myopathic Form Disease MeSH Browser

Myopathic carnitine deficiency Disease MeSH Browser

Myopathy due to Malate-Aspartate Shuttle Defect Disease MeSH Browser

Myopathy with Giant Abnormal Mitochondria Disease MeSH Browser

Myopathy, Cataract, Hypogonadism Syndrome Disease MeSH Browser

Myopathy, Early-Onset, with Fatal Cardiomyopathy Disease MeSH Browser

Myopathy, Granulovacuolar Lobular, with Electrical Myotonia Disease MeSH Browser

Myopathy, X-Linked, with Excessive Autophagy Disease MeSH Browser

Myopathy, congenital nonprogressive with Moebius and Robin sequences Disease MeSH Browser

Myostatin-related muscle hypertrophy Disease MeSH Browser

Neutral Lipid Storage Disease with Myopathy Disease MeSH Browser

Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria Disease MeSH Browser

Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy Disease MeSH Browser

Pectoralis Muscle, Absence of Disease MeSH Browser

Proximal Myopathy with Focal Depletion of Mitochondria Disease MeSH Browser

Rippling muscle disease, 1 Disease MeSH Browser

Singleton Merten syndrome Disease MeSH Browser

Systemic carnitine deficiency Disease MeSH Browser

Tel Hashomer camptodactyly syndrome Disease MeSH Browser

Treft Sanborn Carey syndrome Disease MeSH Browser

Uruguay Faciocardiomusculoskeletal Syndrome Disease MeSH Browser

VLCAD deficiency Disease MeSH Browser

Vacuolar myopathy Disease MeSH Browser

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