Based on "The EMG Expert"
By Björn Falck and Erik Stålberg
Motor neuronopathies
Amyotrophic laterals sclerosis (ALS)
Polio, acute
Polio, sequale following previous paralysis
Spinal muscular atrophy 1, Werdnig-Hoffman
Spinal muscular atrophy 2, Intermediate
Spinal muscular atrophy 3, Kugelberg-Welander
X-linked bulbospinal hereditary neuronopathy (Kennedy syndrome)
Distal spinal muscular atrophy
Monomelic spinal muscular atrophy
Bulbar hereditary motor neuronopathy (Fazio-Londe's disease)
Polyneuropathies
Axonal sensory-motor polyneuropathy
Demyelinating sensory motor polyneuropathy
Acute polyradiculitis (Guillan-Barre Syndrome, GBS, AIDP)
Acute axonal motor neuropathy (AMAN)
Miller-Fisher syndrome
Chronic polyradiculitis (Chronic inflammatory demyelinating polyneuropathy, CIDP)
Multifocal motor neuropathy with conduction block (MMN)
Hereditary motor and sensory neuropathy type 1 (HMSN1, Charcot-Marie-Tooth)
Hereditary motor and sensory neuropathy type 2 (HMSN2, Charcot-Marie-Tooth)
Hereditary motor and sensory neuropathy type 3 (HMSN3, Dejerine-Sottas)
Hereditary motor and sensory neuropathy type 4 (HMSN4, Mb Refsum)
Hereditary neuropathy with liability to pressure palsies (HNPP)
Inherited recurrent brachial plexus neuropathy
Critical illness polyneuropathy
Sensory axonal polyneuropathy
Hereditary sensory polyneuropathy type 1 (Hereditary sensory neuropathy of Denny-Brown)
Hereditary sensory polyneuropathy type 2
Hederitary sensory polyneuropathy type 3 (Familial dysautonomia, Riley-Day syndrome)
Hederitary sensory polyneuropathy type 4 (Congenital sensory neuropathy with anhidrosis)
Tangier disease
Diphtheria
Leprosy (Hansen's disease)
Neuromuscular transmission disorders
Myasthenia gravis (MG)
Neonatal myasthenia gravis
Myasthenic syndrome (Lambert-Eaton myasthenic syndrome, LEMS)
Slow channel syndrome
Congenital acetycholinereceptor (AcR) deficiency
Familial infantile myasthenia
Congenital endplate acetylcholine esterase deficiency (Limb-Girdle myasthenia)
Botulinum intoxication
Myopathies
Inflammatory myopathies
Polymyositis
Dermatomyositis
Inclusion body myositis and inclusion body myopathies (IBM)
Muscular dystrophies
Duchenne muscular dystrophy (DMD)
Becker muscular dystrophy (BMD)
Facio-scapulo-humeral muscular dystrophy (FSHD)
Emery-Dreifuss muscular dystrophy
Limb-girdle muscular dystrophy
Congenital muscular dystrophies
Fukuyama congenital muscular dystrophy
Walker-Warburg sydrome
Muscle eye brain disease (MEB)
Congenital muscular dystrophy with merosin deficiency
Congenital muscular dystrophy with normal merosin
Oculopharyngeal muscular dystrophy
Primary adhalinopathy (a-sarcoglycagonapathy)
Distal myopathies
Late onset distal myopathy type 1 (Welander type)
Late onset distal myopathy type 2 (Markesbury)
Early adult onset distal myopathy type 1
Early adult onset distal myopathy type 2 (Miyoshi)
Tibial muscular dystrophy
Myotonias
Myotonic dystrophy
Proximal myotonic myopathy (PROMM)
Myotonia congenita (Thomsen's form)
Myotonia congenita (Becker's form)
Myotonia fluctuans
Paramyotonia congenita
Chondrosdystrophic myotonia (Schwartz-Jampel syndrome)
Congenital myopathies
Central core disease
Nemaline myopathy
Centronuclear myopathy (myotubular myopathy) neonatal form
Centronuclear myopathy (myotubular myopathy) late infantile-late childhood form
Centronuclear myopathy (myotubular myopathy) late childhood-adult type
Multicore disease
Mini core disease
Fingerprint body myopathy
Hyaline body myopathy
Mitochondrial myopathies
Myoclonic epilepsy and ragged red fibers (MERFF)
Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)
Succinate dehydrogenase deficiency (complex II deficiency)
Fatal infantile myopathy with cytochrome c oxidase deficiency (complex IV deficiency)
Benign infantile myopathy with cytochrome c oxidase deficiency (complex IV deficiency)
Leigh's syndrome
Kearns-Sayre syndrome
Familial progressive external ophtalmoplegia (PEO) syndrome
Late onset mitochondrial myopathy
Metabolic myopathies
Acid maltase deficiency (Pompe's disease, glycogenosis type 2)
Debranching enzyme deficiency (glycogenosis type 3)
Branching enzyme deficiency (glycogenosis type 4)
Myophosphorylase deficiency (McArdles's disese.glucogenosis type 5)
Phosphofructokinase deficiency (Tarui's disease, glycogenosis type 7)
Phosphoglycerate kinase deficiency (glycogenosis type 9)
Phosphoglycerate mutase deficiency (glycogenosis type 10)
Lactate dehydrogenase deficiency (glycogenosis type 11)
Carnitine deficiency
Carnitine palmityl transferase deficiency
Myoadenylate deaminase deficiency
Primary periodic paralysis
Hypokalemic periodic paralysis
Hyperkalemic periodic paralysis
Miscellaneous myopathies
Bent spine syndrome (Isolated neck extensor myopathy)
Malignant hypertermia
Neuroleptic malignant syndrome
Rippling muscle disease
Local nerve lesions
Shoulder, neck and upper extremeties
Median nerve
Carpal tunnel syndrome (CTS)
Median nerve lesion above the wrist
Anterior interosseus nerve lesion
Median nerve lesion around the elbow
Median nerve lesion above the elbow
Radial nerve
Radial nerve lesion in the upper arm
Radial nerve lesion in the axilla
Posterior interosseus nerve lesion
Lesion of the sensory radial nerve the forearm
Ulnar nerve
Ulnar nerve lesion at the wrist
Ulnar nerve lesion in the cubital tunnel
Ulnar nerve lesion at the medial epicondyle
Deep motor branch of the ulnar nerve lesion at the wrist
Superficial sensory branch of the ulnar nerve lesion at the wrist
Other nerves
Subscapular nerve lesion
Suprascapular nerve lesion
Axillary nerve lesion
Musculocutaneous nerve lesion
Thoracodorsal nerve lesion
Phrenic nerve lesions
Long thoracic nerve lesion
Dorsal scapular nerve lesion
Brachial plexus lesions
Lateral cutaneous nerve of the forearm lesion
Medial cutaneous nerve of the forearm lesion
Cranial nerves
Oculomotor nerve lesion (III)
Trochlear nerve lesion (IV)
Trigeminal nerve lesions (V)
Inferior alveolar nerve lesion (V)
Lingual nerve lesion (V)
Abducens nerve lesion (VI)
Facial nerve lesion (VII)
Glossopharyngeal nerve lesion (IX)
Vagus nerve lesion (X)
Recurrent nerve lesion (X)
Accessory nerve lesion (XI)
Hypoglossal nerve lesion (XII)
Lower extremeties
Lumbal plexus and its nerves
Lumbal plexus lesion
Sacral plexus lesion
Genitofemoral nerve lesion
Ilioinguinal nerve lesion
Iliohypogastric nerve lesion
Obturator nerve lesion
Femoral nerve lesion
Saphenous nerve lesion
Lesion of the lateral cutaneous nerve of the thigh (Meralgia paresthetica)
Lumbosacral plexus, sciatic nerve and its branches
Lumbosacral plexus lesion
Sciatic nerve lesion
Pudendal nerve lesion
Common peroneal nerve lesion at the knee
Superficial peroneal nerve lesion in the foot
Posterior cutaneous femoral nerve lesion
Sural nerve lesion in the calf
Sural nerve lesion at the malleolus
Sural nerve lesion at the knee
Tarsal tunnel syndrome
Anterior tarsal tunnel syndrome
Morton's metatarsalgia
Radiculopathies
Cervical radiculopathies
C1 radiculopathy
C2 radiculopathy
C3 radiculopathy
C4 radiculopathy
C5 radiculopathy
C6 radiculopathy
C7 radiculopathy
C8 radiculopathy
Lumbal and sacral radiculopathies
L1 radiculopathy
L2 radiculopathy
L3 radiculopathy
L4 radiculopathy
L5 radiculopathy
S1 radiculopathy
Thoracic radiculopathies
Th1 radiculopathy
Th2-Th10 radiculopathy
Th11 radiculopathy
Th12 radiculopathy
No radiculopathies
Neck pain with no radiculopathy
Low back pain with no radiculopathy
Disorders of the spinal chord and central nervous system with neuromuscular abnormalities
Cervical syringomyelia
Friedreich's ataxia
Machado-Joseph disease
Metachromatic leukodystrophy
Galactosylceramide lipidosis (Krabbe disease, globoid cell dystrophy)
Adrenoleukodystrophy/adrenomyeloneuropathy
Miscellaneous
Benign fasciculation
Neuromyotonia (Isaac's syndrome, continous muscle fiber activity)
Stiff man syndrome
Tetanus
Symptoms
Diseases