Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Hereditary neurological disease · Neuromuscular disease

Hereditary neuromuscular disease

A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that is characterized by progressive muscle degeneration and weakness.

3 trials tagged with this condition →

Hereditary peripheral neuropathy 6 trials · 478 incl. sub-types Sub-types →
Muscular dystrophy 74 trials · 288 incl. sub-types Sub-types →
Hereditary motor neuron disease 1 trial · 169 incl. sub-types Sub-types →
Hereditary spastic paraplegia 27 trials · 33 incl. sub-types Sub-types →
Benign paroxysmal positional vertigo 18 trials
Meniere disease 16 trials Sub-types →
RYR1-related myopathy 5 trials · 6 incl. sub-types Sub-types →
Congenital myasthenic syndrome 5 trials Sub-types →
Malignant hyperthermia of anesthesia 5 trials
SCN4A-related channelopathy 1 trial · 2 incl. sub-types Sub-types →
Early-onset myopathy with fatal cardiomyopathy 1 trial
Andersen-Tawil syndrome 0 trials
CNGB3-related retinopathy 0 trials Sub-types →
KY-related neuromyopathy 0 trials Sub-types →
Morimoto-Ryu-Malicdan neuromuscular syndrome 0 trials
X-linked recessive mitochondrial myopathy 0 trials
Myofibrillar myopathy 1 0 trials
Myotonia congenita, autosomal dominant 0 trials
Myotonia congenita, autosomal recessive 0 trials
Neuromuscular disorder, congenital, with dysmorphic facies 0 trials
Periodic paralysis with later-onset distal motor neuropathy 0 trials
Vertigo, benign recurrent, 1 0 trials