nemoci svalů [Muscular Diseases]

tematický
553
Termíny

choroby svalů
myopatie
onemocnění svalů
svaly - nemoci

 

Muscle Disorders
Myopathic Conditions
Myopathies

Perzistentní odkaz   https://www.medvik.cz/link/D009135
Definice

Získané, dědičné a vrozené poruchy kosterního a hladkého svalstva (SVALY KOSTERNÍ, SVALY HLADKÉ).

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

Anotace
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 Prohlížeč
CUI
M0014252

C Nemoci
C05.116 nemoci kostí 792
C05.182 nemoci chrupavky 140
C05.321 fasciitida 41
C05.390 deformity ruky 51
C05.500 nemoci čelistí 134
C05.550 nemoci kloubů 1 253
C05.651 nemoci svalů 553
C05.651.102 artrogrypóza 31
C05.651.180 kompartment syndrom 113
C05.651.197 kontraktura 154
C05.651.324 fibromyalgie 133
C05.651.392 Isaacsův syndrom 7
C05.651.475 svalové křeče 176
C05.651.494 nádory svalů 17
C05.651.504 svalová rigidita 47
C05.651.512 svalová spasticita 457
C05.651.515 svalová slabost 224
C05.651.534 svalové atrofie 45
C05.651.542 myalgie 53
C05.651.594 myozitida 250
C05.651.662 myotonické poruchy 23
C05.651.682 myotoxicita 1
C05.651.742 polymyalgia rheumatica 110
C05.651.807 rhabdomyolýza 128
C05.651.869 tendinopatie 90
C05.799 revmatické nemoci 2 175
C10.668.416 syndrom uzamčení 3
C10.668.491 nemoci svalů 553
C10.668.491.175 svalové atrofie 45
C10.668.491.425 fibromyalgie 133
C10.668.491.500 mitochondriální myopatie 40
C10.668.491.525 myalgie 53
C10.668.491.562 myozitida 250
C10.668.491.606 myotonické poruchy 23
C10.668.491.628 myotoxicita 1
C10.668.864 poliomyelitida 476

Alpha-B Crystallinopathy Disease MeSH Prohlížeč

Anal Sphincter Myopathy, Internal Disease MeSH Prohlížeč

Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy Disease MeSH Prohlížeč

Carnitine Palmitoyltransferase II Deficiency, Late-Onset Disease MeSH Prohlížeč

Chanarin-Dorfman Syndrome Disease MeSH Prohlížeč

Dimauro disease Disease MeSH Prohlížeč

Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts Disease MeSH Prohlížeč

Epiphyseal Dysplasia, Multiple, with Myopathy Disease MeSH Prohlížeč

Erythrocyte Amp Deaminase Deficiency Disease MeSH Prohlížeč

Erythrocyte Lactate Transporter Defect Disease MeSH Prohlížeč

Fingerprint Body Myopathy Disease MeSH Prohlížeč

Hereditary Myopathy with Early Respiratory Failure Disease MeSH Prohlížeč

Hypertrophia Musculorum Vera Disease MeSH Prohlížeč

Kocher-Debre-Semelaigne syndrome Disease MeSH Prohlížeč

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

Mitochondrial DNA Depletion Syndrome, Myopathic Form Disease MeSH Prohlížeč

Myopathic carnitine deficiency Disease MeSH Prohlížeč

Myopathy due to Malate-Aspartate Shuttle Defect Disease MeSH Prohlížeč

Myopathy with Giant Abnormal Mitochondria Disease MeSH Prohlížeč

Myopathy, Cataract, Hypogonadism Syndrome Disease MeSH Prohlížeč

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

Myopathy, Granulovacuolar Lobular, with Electrical Myotonia Disease MeSH Prohlížeč

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

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

Myostatin-related muscle hypertrophy Disease MeSH Prohlížeč

Neutral Lipid Storage Disease with Myopathy Disease MeSH Prohlížeč

Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria Disease MeSH Prohlížeč

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

Pectoralis Muscle, Absence of Disease MeSH Prohlížeč

Proximal Myopathy with Focal Depletion of Mitochondria Disease MeSH Prohlížeč

Rippling muscle disease, 1 Disease MeSH Prohlížeč

Singleton Merten syndrome Disease MeSH Prohlížeč

Systemic carnitine deficiency Disease MeSH Prohlížeč

Tel Hashomer camptodactyly syndrome Disease MeSH Prohlížeč

Treft Sanborn Carey syndrome Disease MeSH Prohlížeč

Uruguay Faciocardiomusculoskeletal Syndrome Disease MeSH Prohlížeč

VLCAD deficiency Disease MeSH Prohlížeč

Vacuolar myopathy Disease MeSH Prohlížeč