You are using an outdated browser. Please upgrade your browser to improve your experience.

genetic peripheral neuropathy

Disease Summary
Associated Targets (468)
Tbio

325

Tchem

69

Tclin

65

Tdark

9


Explore Associated Targets
Mondo Description Genetic peripheral neuropathy.
Mondo Term and Equivalent IDs
MONDO:0020127:  genetic peripheral neuropathy
Orphanet:98497: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
genetic nervous system disorder (6096)
Tbio

4331

Tchem

803

Tdark

604

Tclin

358

peripheral neuropathy (992)
Tbio

660

Tchem

178

Tclin

123

Tdark

31

Children
Charcot-Marie-Tooth disease (225)
Tbio

161

Tchem

37

Tclin

26

Tdark

1

mitochondrial disease with peripheral neuropathy (98)
Tbio

63

Tclin

24

Tchem

9

Tdark

2

hereditary motor and sensory neuropathy (53)
Tbio

43

Tchem

8

Tclin

2

carpal tunnel syndrome (48)
Tbio

38

Tclin

4

Tdark

4

Tchem

2

hereditary sensory and autonomic neuropathy (41)
Tbio

26

Tchem

8

Tclin

7

Wilson disease (27)
Tbio

15

Tchem

9

Tclin

3

peroxisome biogenesis disorder (20)
Tbio

19

Tchem

1

distal hereditary motor neuropathy (16)
Tbio

10

Tchem

5

Tclin

1

Finnish type amyloidosis (8)
Tbio

5

Tchem

2

Tclin

1

cerebellar ataxia with peripheral neuropathy (8)
Tbio

8

proximal spinal muscular atrophy (7)
Tbio

6

Tchem

1

adult Refsum disease (6)
Tbio

6

adrenomyeloneuropathy (6)
Tbio

4

Tclin

1

Tchem

1

abetalipoproteinemia (5)
Tclin

4

Tchem

1

metachromatic leukodystrophy (4)
Tbio

4

Tay-Sachs disease (3)
Tchem

1

Tbio

1

Tdark

1

tyrosinemia type I (3)
Tbio

2

Tclin

1

familial isolated deficiency of vitamin E (3)
Tchem

2

Tbio

1

spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 (3)
Tchem

2

Tbio

1

long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (3)
Tbio

2

Tdark

1

familial episodic pain syndrome (3)
Tclin

3

giant axonal neuropathy (2)
Tbio

2

chorea-acanthocytosis (2)
Tbio

2

Tangier disease (2)
Tclin

1

Tbio

1

Tangier disease (2)
Tclin

1

Tbio

1

Chediak-Higashi syndrome (2)
Tbio

2

triple-A syndrome (2)
Tbio

2

Sandhoff disease (2)
Tchem

1

Tbio

1

Fabry disease (2)
Tclin

1

Tchem

1

Niemann-Pick disease type B (2)
Tclin

1

Tchem

1

PCWH syndrome (2)
Tbio

2

neuropathy, congenital hypomelinating (2)
Tbio

2

familial amyloid neuropathy (1)
Tclin

1

episodic ataxia type 1 (1)
Tclin

1

amyotrophic neuralgia (1)
Tchem

1

cerebrotendinous xanthomatosis (1)
Tchem

1

homocystinuria due to methylene tetrahydrofolate reductase deficiency (1)
Tbio

1

Krabbe disease (1)
Tbio

1

beta-mannosidosis (1)
Tchem

1

biotinidase deficiency (1)
Tbio

1

ornithine aminotransferase deficiency (1)
Tchem

1

adult polyglucosan body disease (1)
Tbio

1

methylmalonic aciduria and homocystinuria type cblC (1)
Tbio

1

primary CD59 deficiency (1)
Tbio

1

PHARC syndrome (1)
Tchem

1

progressive demyelinating neuropathy with bilateral striatal necrosis (1)
Tbio

1

cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome (1)
Tchem

1

ataxia - oculomotor apraxia type 4 (1)
Tchem

1

sodium channelopathy-related small fiber neuropathy (1)
Tclin

1

attenuated Chédiak-Higashi syndrome (1)
Tbio

1

spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 (1)
Tbio

1

neurodegeneration with brain iron accumulation 2A (1)
Tchem

1

congenital trigeminal anesthesia (0)
familial recurrent peripheral facial palsy (0)
meralgia paraesthetica, familial (0)
infantile axonal neuropathy (0)
non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy (0)
optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome (0)
EMILIN-1-related connective tissue disease (0)
optic atrophy-peripheral neuropathy-developmental delay syndrome (0)
PRPS1 deficiency disorder (0)
Target Novelty (Tin-x)
No novelty measurements found