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Autoimmune necrotising myopathy
Congenital muscular dystrophy NOS
Congenital myopathies
Disease central core
Hypoparathyroidism
Minicore
Multicore
Muscle diease
Myopathie
Myopathy
Myopathy in hyperparathyroidism
Nemaline
Nemaline myopathy
Thyrotoxic myopathy

Vertaling van "myopathy " (Engels → Nederlands) :





Myopathy in:hyperparathyroidism (E21.0-E21.3+) | hypoparathyroidism (E20.-+) | Thyrotoxic myopathy (E05.-+)

myopathie bij | hyperparathyroïdie (E21.0-E21.3) | myopathie bij | hypoparathyroïdie (E20.-) | thyrotoxische myopathie (E05.-)




A rare genetic mitochondrial oxidative phosphorylation disorder with characteristics of either late-onset myopathy with progressive external ophthalmoplegia and muscular weakness (predominantly limb-girdle) or early-onset myopathy presenting with dec

DNA2-gerelateerd mitochondriaal DNA-deletiesyndroom




A rare genetic, non-dystrophic myopathy with characteristics of fatigable muscle weakness associated with congenital myopathy. Patients present with axial hypotonia, myopathic facies with fatigable ptosis, feeding difficulties, delayed gross motor de

congenitale myopathie met myasthenie-achtige aanvang




Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes


Autoimmune necrotising myopathy

auto-immune necrotiserende myopathie




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Date index: 2024-08-25
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