Hereditary peripheral neuropathy

Part of

Sub-types of Hereditary peripheral neuropathy

• Carpal tunnel syndrome 165 trials
  2 sub-types

  • Carpal tunnel syndrome 1 0 trials
  • Carpal tunnel syndrome 2 0 trials
• Charcot-Marie-Tooth disease 52 trials · 78 incl. sub-types
  24 sub-types

  • Charcot-Marie-Tooth disease type 1 4 trials · 40 incl. sub-types Sub-types →
  • Charcot-Marie-Tooth disease type 2 3 trials · 9 incl. sub-types Sub-types →
  • Charcot-Marie-Tooth disease type 4 0 trials · 5 incl. sub-types Sub-types →
  • Intermediate Charcot-Marie-Tooth disease 0 trials · 3 incl. sub-types Sub-types →
  • Charcot-Marie-Tooth disease type X 1 trial · 2 incl. sub-types Sub-types →
  • Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b; 1 trial
  • Charcot-Marie-Tooth disease type 3 0 trials
  • Charcot-Marie-Tooth disease with ptosis and parkinsonism 0 trials
  • Charcot-Marie-Tooth disease, Guadalajara neuronal type 0 trials
  • Charcot-Marie-Tooth disease, axonal, IIa 2II 0 trials
  • Charcot-Marie-Tooth disease, axonal, Type 2HH 0 trials
  • Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1 0 trials
  • Charcot-Marie-Tooth disease, axonal, type 2FF 0 trials
  • Charcot-Marie-Tooth disease, axonal, type 2KK 0 trials
  • Charcot-Marie-Tooth disease, axonal, type 2LL 0 trials
  • Charcot-Marie-Tooth disease, demyelinating, IIA 1H 0 trials
  • Charcot-Marie-Tooth disease, demyelinating, IIA 1I 0 trials
  • Charcot-Marie-Tooth disease, demyelinating, type 1G 0 trials
  • Charcot-Marie-Tooth disease, demyelinating, type 1J 0 trials
  • Charcot-Marie-tooth disease, axonal, type 2JJ 0 trials
  • Charcot-marie-tooth disease, axonal, type 2MM 0 trials
  • Demyelinating hereditary motor and sensory neuropathy 0 trials
  • Neuronopathy, distal hereditary motor, autosomal dominant 1 0 trials
  • Neuropathy, hereditary motor and sensory, type 6A 0 trials
• Familial amyloid neuropathy 52 trials · 54 incl. sub-types
  4 sub-types

  • Amyloidosis, hereditary systemic 1 0 trials · 10 incl. sub-types Sub-types →
  • Amyloidosis, hereditary systemic 3 0 trials
  • Amyloidosis, hereditary systemic 5 0 trials
  • Amyloidosis, hereditary systemic 6 0 trials
• Hereditary sensory and autonomic neuropathy 52 trials · 54 incl. sub-types
  13 sub-types

  • Hereditary sensory and autonomic neuropathy type 1 0 trials · 2 incl. sub-types Sub-types →
  • X-linked hereditary sensory and autonomic neuropathy with hearing loss 0 trials
  • Cold-induced sweating syndrome - hyperthermia spectrum 0 trials Sub-types →
  • Congenital insensitivity to pain with hyperhidrosis 0 trials
  • Congenital insensitivity to pain-hypohidrosis syndrome 0 trials
  • Hereditary sensory and autonomic neuropathy type 2 0 trials Sub-types →
  • Hereditary sensory and autonomic neuropathy type 4 0 trials
  • Hereditary sensory and autonomic neuropathy type 5 0 trials
  • Hereditary sensory and autonomic neuropathy type 6 0 trials
  • Hereditary sensory and autonomic neuropathy type 7 0 trials
  • Hereditary sensory neuropathy X-linked 0 trials
  • Neuropathy, hereditary sensory, atypical 0 trials
  • Polyneuropathy-hand defect syndrome 0 trials
• Proximal spinal muscular atrophy 14 trials · 42 incl. sub-types
  6 sub-types

  • Spinal muscular atrophy, type 1 17 trials
  • Spinal muscular atrophy, type II 14 trials
  • Spinal muscular atrophy, type III 13 trials
  • Spinal muscular atrophy, type IV 2 trials
  • Autosomal dominant childhood-onset proximal spinal muscular atrophy 0 trials Sub-types →
  • Lower motor neuron syndrome with late-adult onset 0 trials
• Metachromatic leukodystrophy 20 trials
  2 sub-types

  • Metachromatic leukodystrophy, juvenile form 2 trials · 4 incl. sub-types Sub-types →
  • Metachromatic leukodystrophy due to saposin B deficiency 0 trials
• Krabbe disease 15 trials
  3 sub-types

  • Infantile Krabbe disease 2 trials
  • Adult Krabbe disease 0 trials
  • Late-infantile/juvenile Krabbe disease 0 trials
• Sandhoff disease 13 trials
  3 sub-types

  • Sandhoff disease, adult form 1 trial
  • Sandhoff disease, infantile form 0 trials
  • Sandhoff disease, juvenile form 0 trials
• Tay-Sachs disease 13 trials
  4 sub-types

  • Tay-Sachs disease, B variant, adult form 3 trials
  • Tay-Sachs disease, b variant, juvenile form 1 trial
  • Tay-Sachs disease, B1 variant 0 trials
  • Tay-Sachs disease, b variant, infantile form 0 trials
• Chediak-Higashi syndrome 9 trials
• Leigh syndrome 9 trials
  4 sub-types

  • Maternally-inherited Leigh syndrome 1 trial
  • Leigh syndrome with cardiomyopathy 0 trials
  • Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type 0 trials
  • Necrotizing encephalomyelopathy, subacute, of Leigh, adult 0 trials
• Peroxisome biogenesis disorder 4 trials · 8 incl. sub-types
  2 sub-types

  • Zellweger spectrum disorders 6 trials · 7 incl. sub-types Sub-types →
  • Non-Zellweger spectrum disorder 0 trials · 1 incl. sub-types Sub-types →
• Adrenomyeloneuropathy 7 trials
• Cerebrotendinous xanthomatosis 6 trials
• Kearns-Sayre syndrome 5 trials
• Hereditary neuropathy with liability to pressure palsies 4 trials
• Mitochondrial neurogastrointestinal encephalomyopathy 4 trials
  4 sub-types

  • Mitochondrial DNA depletion syndrome 1 0 trials
  • Mitochondrial DNA depletion syndrome 20 (mngie type) 0 trials
  • Mitochondrial DNA depletion syndrome 4b 0 trials
  • Mitochondrial DNA depletion syndrome 8a 0 trials
• Ornithine aminotransferase deficiency 4 trials
• Pyruvate dehydrogenase deficiency 2 trials · 4 incl. sub-types
  7 sub-types

  • Pyruvate dehydrogenase E1-alpha deficiency 2 trials
  • Pyruvate dehydrogenase E3 deficiency 1 trial
  • Lipoic acid synthetase deficiency 0 trials
  • Pyruvate dehydrogenase E1-beta deficiency 0 trials
  • Pyruvate dehydrogenase E2 deficiency 0 trials
  • Pyruvate dehydrogenase E3-binding protein deficiency 0 trials
  • Pyruvate dehydrogenase phosphatase deficiency 0 trials
• Distal hereditary motor neuropathy 0 trials · 4 incl. sub-types
  3 sub-types

  • Neuronopathy, distal hereditary motor, autosomal recessive 0 trials · 4 incl. sub-types Sub-types →
  • X-linked distal spinal muscular atrophy type 3 0 trials
  • Neuronopathy, distal hereditary motor, autosomal dominant 0 trials Sub-types →
• NARP syndrome 3 trials
• Biotinidase deficiency 3 trials
• Coenzyme Q10 deficiency 3 trials
  10 sub-types

  • COQ7-related distal hereditary motor neuropathy 0 trials
  • Autosomal recessive ataxia due to ubiquinone deficiency 0 trials
  • Coenzyme Q10 deficiency, primary, 1 0 trials
  • Coenzyme Q10 deficiency, primary, 3 0 trials
  • Coenzyme q10 deficiency, primary, 9 0 trials
  • Deafness-encephaloneuropathy-obesity-valvulopathy syndrome 0 trials
  • Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome 0 trials
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness 0 trials
  • Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome 0 trials
  • Primary coenzyme Q10 deficiency 8 0 trials
• Hereditary motor and sensory neuropathy 3 trials
  8 sub-types

  • Autosomal dominant slowed nerve conduction velocity 0 trials
  • Demyelinating hereditary motor and sensory neuropathy 0 trials
  • Hereditary motor and sensory neuropathy type 6 0 trials Sub-types →
  • Hereditary motor and sensory neuropathy with acrodystrophy 0 trials
  • Hereditary sensorimotor neuropathy with hyperelastic skin 0 trials
  • Hereditary thermosensitive neuropathy 0 trials
  • Polyneuropathy-hand defect syndrome 0 trials
  • Severe early-onset axonal neuropathy due to MFN2 deficiency 0 trials
• Methylmalonic aciduria and homocystinuria type cblC 3 trials
• Mitochondrial DNA depletion syndrome 4a 3 trials
• Giant axonal neuropathy 2 trials · 3 incl. sub-types
  2 sub-types

  • Giant axonal neuropathy 1 1 trial
  • Giant axonal neuropathy 2 0 trials
• Abetalipoproteinemia 2 trials
• Fumaric aciduria 2 trials
• Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 2 trials
• Niemann-Pick disease type B 1 trial
• PRPS1 deficiency disorder 1 trial
• Adult polyglucosan body disease 1 trial
• Familial isolated deficiency of vitamin E 1 trial
• Homocystinuria due to methylene tetrahydrofolate reductase deficiency 1 trial
• Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 1 trial
• Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 1 trial
  1 sub-type

  • Spinocerebellar ataxia with epilepsy 1 trial
• Neuropathy, congenital hypomelinating 0 trials · 1 incl. sub-types
  3 sub-types

  • Charcot-Marie-Tooth disease type 4E 1 trial
  • Neuropathy, congenital hypomyelinating, 2 0 trials
  • Neuropathy, congenital hypomyelinating, 3 0 trials
• Charcot-Marie-Tooth disease type 5 0 trials
• EMILIN-1-related connective tissue disease 0 trials
• Finnish type amyloidosis 0 trials
• PHARC syndrome 0 trials
• VPS13A-related neurodegenerative disease 0 trials
• Amyotrophic neuralgia 0 trials
• Ataxia - oculomotor apraxia type 4 0 trials
• Attenuated Chédiak-Higashi syndrome 0 trials
• Beta-mannosidosis 0 trials
• Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome 0 trials
• Congenital trigeminal anesthesia 0 trials
• Familial episodic pain syndrome 0 trials
  3 sub-types

  • Episodic pain syndrome, familial, 2 0 trials
  • Familial episodic pain syndrome with predominantly lower limb involvement 0 trials
  • Familial episodic pain syndrome with predominantly upper body involvement 0 trials
• Familial recurrent peripheral facial palsy 0 trials
• Hereditary motor and sensory neuropathy, Okinawa type 0 trials
  1 sub-type

  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation 0 trials
• Hereditary sensory and autonomic neuropathy with spastic paraplegia 0 trials
• Infantile axonal neuropathy 0 trials
• Meralgia paraesthetica, familial 0 trials
• Neurodegeneration with brain iron accumulation 2A 0 trials
• Neuropathy with hearing impairment 0 trials
• Neuropathy, hereditary sensory and autonomic, type IId 0 trials
• Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy 0 trials
• Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome 0 trials
• Oxoglutaricaciduria 0 trials
• Peripheral motor neuropathy, childhood-onset, biotin-responsive 0 trials
• Primary CD59 deficiency 0 trials
• Progressive demyelinating neuropathy with bilateral striatal necrosis 0 trials
• Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 0 trials