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Up to: Peripheral neuropathy · Hereditary neuromuscular disease

Hereditary peripheral neuropathy

An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual.

6 trials tagged with this condition →

Carpal tunnel syndrome 165 trials Sub-types →
Charcot-Marie-Tooth disease 51 trials · 77 incl. sub-types Sub-types →
Familial amyloid neuropathy 52 trials · 54 incl. sub-types Sub-types →
Hereditary sensory and autonomic neuropathy 52 trials · 54 incl. sub-types Sub-types →
Proximal spinal muscular atrophy 14 trials · 42 incl. sub-types Sub-types →
Metachromatic leukodystrophy 20 trials Sub-types →
Krabbe disease 15 trials Sub-types →
Sandhoff disease 13 trials Sub-types →
Tay-Sachs disease 13 trials Sub-types →
Chediak-Higashi syndrome 9 trials
Leigh syndrome 9 trials Sub-types →
Peroxisome biogenesis disorder 4 trials · 8 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 Sub-types →
Ornithine aminotransferase deficiency 4 trials
Pyruvate dehydrogenase deficiency 2 trials · 4 incl. sub-types Sub-types →
Distal hereditary motor neuropathy 0 trials · 4 incl. sub-types Sub-types →
NARP syndrome 3 trials
Biotinidase deficiency 3 trials
Coenzyme Q10 deficiency 3 trials Sub-types →
Hereditary motor and sensory neuropathy 3 trials Sub-types →
Methylmalonic aciduria and homocystinuria type cblC 3 trials
Mitochondrial DNA depletion syndrome 4a 3 trials
Giant axonal neuropathy 2 trials · 3 incl. sub-types Sub-types →
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 Sub-types →
Neuropathy, congenital hypomelinating 0 trials · 1 incl. sub-types Sub-types →
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 Sub-types →
Familial recurrent peripheral facial palsy 0 trials
Hereditary motor and sensory neuropathy, Okinawa type 0 trials Sub-types →
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