Myopathies, Structural, Congenital [myopatie strukturální vrozené]
- Terms
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centronukleární myopatie
centronukleární myopatie 1
centronukleární myopatie autozomálně dominantní
centronukleární myopatie autozomálně recesivní
myotubulární myopatie
myotubulární myopatie autozomálně dominantní
myotubulární myopatie vázaná na chromozom X
strukturální vrozené myopatie
tubulární agregátová myopatie
vrozená disproporce typu vláken
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Autosomal Dominant Myotubular Myopathy
Autosomal Recessive Centronuclear Myopathy
Centronuclear Myopathy
CFTDM
Congenital Fiber Type Disproportion
Congenital Fiber-Type Disproportion
Congenital Myopathy with Fiber Type Disproportion
Congenital Non-Progressive Myopathies
Congenital Structural Myopathies
Fiber-Type Disproportion Myopathy, Congenital
Myopathy, Centronuclear, 1
Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Congenital, With Fiber-Type Disproportion
Myopathy, Myotubular
Myopathy, Tubular Aggregate
Myotubular Myopathy
Myotubular Myopathy 1
Myotubular Myopathy, Autosomal Dominant
Myotubular Myopathy, X-Linked
Non-Progressive Myopathies, Congenital
Structural Myopathies, Congenital
Tubular Aggregate Myopathy
X-Linked Centronuclear Myopathy
X-Linked Myotubular Myopathy
XLMTM
A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality.
- DUI
- D020914 MeSH Browser
- CUI
- M0328270
- Previous indexing
- Muscular Atrophy (1976-1999); Neuromuscular Diseases (1976-1999)
- History note
- 2000
- Public note
- 2000
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications
- CN
- congenital
- DI
- diagnosis 3
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics 7
- HI
- history
- IM
- immunology
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 1
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 3
- UR
- urine
- VE
- veterinary
- VI
- virology
Actin-Accumulation Myopathy Disease MeSH Browser
Cap Myopathy Disease MeSH Browser
Minicore Myopathy with External Ophthalmoplegia Disease MeSH Browser
Myofibrillar Myopathy Disease MeSH Browser
Myopathy, Centronuclear, Autosomal Recessive Disease MeSH Browser
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Disease MeSH Browser
Myopathy, Myofibrillar, Bag3-Related Disease MeSH Browser
Myosclerosis, Autosomal Recessive Disease MeSH Browser
Myotilinopathy Disease MeSH Browser
Myotubular Myopathy with Abnormal Genital Development Disease MeSH Browser
Pleoconial Myopathy with Salt Craving Disease MeSH Browser
Spheroid body myopathy Disease MeSH Browser