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About:
clgo:
Neuromuscular_disorder
Property
Value
rdf:
type
owl:
Class
rdfs:
label
Neuromuscular disorder
rdfs:
subClassOf
Disease
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Neuromuscular_disorders
http://en.wikipedia.org/wiki/List_of_neuromuscular_disorders
is
rdf:
type
of
Amyotrophic lateral sclerosis
Spinal and bulbar muscular atrophy
Multi/minicore myopathy
Radial neuropathy
Tarsal tunnel syndrome
Ulnar neuropathy
Genitofemoral nerve
Carpal tunnel syndrome
Congenital fiber type disproportion
LGMD R23 laminin α2-
R20 ISPD
LAMA2-related (merosin deficient) congenital muscular dystrophy
Spinal muscular atrophy with lower extremity predominance 1
Dermatomyositis
Iliohypogastric nerve
Cerebral palsy
Centronuclear myopathy
Becker muscular dystrophy
Mitochondrial encephalomyopathy
Hereditary spastic paraplegia
Congenital myasthenic syndrome
Duchenne muscular dystrophy
Spinal muscular atrophy
Herpes simplex virus
Myotonic dystrophy
Facioscapulohumeral muscular dystrophy
Nemaline myopathy
Statin-associated autoimmune myopathy
Chemotherapy-induced peripheral neuropathy
Inclusion body myositis
TRAPPC9
Kearns–Sayre syndrome
Morton's neuroma
sciatic mononeuroapthy
Spine
R17 plectin
Collagen VI-related muscular dystrophy
Bag3opathy
Emery–Dreifuss muscular dystrophy
Cramp fasciculation syndrome
Desmin-related myofibrillar myopathy
Ilioinguinal nerve
Myasthenia gravis
Myoclonic epilepsy
Zaspopathy
Suprascapular nerve
Lambert–Eaton myasthenic syndrome
Mononeuropathy
Femoral neuropathy
Myotilinopathy
Fukutin-
Cylindrical spirals myopathy
Mitochondrial complex II deficiency
Carnitine palmitoyltransferase I deficiency
Distal spinal muscular atrophy type 1
Trigeminal neuralgia
Vagus nerve
glomus jugulare
sural mononeuropathy
R11 POMT1-
R22 collagen 6-
Troyer syndrome
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Facial onset sensory and motor neuronopathy
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Carnitine palmitoyltransferase II deficiency
Glossopharyngeal nerve
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Charcot–Marie–Tooth disease
Guillain–Barré syndrome
Spinocerebellar ataxia
Polymyositis
Piriformis syndrome
Spinal muscular atrophy with lower extremity predominance 2A
Facial nerve
Bell's palsy
Dilated cardiomyopathy
Cytochrome c oxidase (COX) deficiency
mtDNA deletion
Glycogen storage disease type II
Phosphoglycerate kinase
Möbius syndrome
Trigeminal nerve
Spinal muscular atrophy with lower extremity predominance 2B
X-linked spinal muscular atrophy type 2
Axillary neuropathy
GSD Ib
Idiopathic facial palsy
neuropathy of gluteal nerves
Glossopharyngeal neuralgia
R19 GMPPB
R12 anoctamin5-
Tibial neuropathy
obturator neuropathy
LGMD1H
Late adult-onset type 1
Numbness
Filaminopathy
Long thoracic neuropathy
Isaacs–Mertens syndrome
... and more