PomBase home

Disease association ontology term - MONDO:0020127 - hereditary peripheral neuropathy

Term summary

ID
MONDO:0020127
Name
hereditary peripheral neuropathy
Ontology or CV name
Disease association
Definition
An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual.

Parents

Annotation

Disease association

MONDO:0971004 - amyloidosis, hereditary systemic 1

References:

Genes:

MONDO:0008076 - amyotrophic neuralgia

References:

Genes:

MONDO:0014557 - ataxia - oculomotor apraxia type 4

References:

Genes:

MONDO:0014711 - autosomal dominant Charcot-Marie-Tooth disease type 2W

References:

Genes:

MONDO:0008026 - autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

References:

Genes:

MONDO:0012784 - autosomal recessive ataxia due to ubiquinone deficiency

References:

Genes:

MONDO:0011436 - autosomal recessive distal spinal muscular atrophy 1

References:

Genes:

MONDO:0011585 - autosomal recessive distal spinal muscular atrophy 2

References:

Genes:

MONDO:0020730 - carpal tunnel syndrome 1

References:

Genes:

MONDO:0014455 - cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

References:

Genes:

MONDO:0044720 - cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

References:

Genes:

MONDO:0015626 - Charcot-Marie-Tooth disease

References:

Genes:

MONDO:0011687 - Charcot-Marie-Tooth disease axonal type 2F

References:

Genes:

MONDO:0012096 - Charcot-Marie-Tooth disease axonal type 2L

References:

Genes:

MONDO:0013212 - Charcot-Marie-Tooth disease axonal type 2N

References:

Genes:

MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

References:

Genes:

MONDO:0014511 - Charcot-Marie-Tooth disease axonal type 2S

References:

Genes:

MONDO:0014566 - Charcot-Marie-Tooth disease axonal type 2U

References:

Genes:

MONDO:0012012 - Charcot-Marie-Tooth disease dominant intermediate C

References:

Genes:

MONDO:0014074 - Charcot-Marie-Tooth disease dominant intermediate F

References:

Genes:

MONDO:0013338 - Charcot-Marie-Tooth disease recessive intermediate B

References:

Genes:

MONDO:0014467 - Charcot-Marie-Tooth disease recessive intermediate D

References:

Genes:

MONDO:0012231 - Charcot-Marie-Tooth disease type 2A2

References:

Genes:

MONDO:0010949 - Charcot-Marie-Tooth disease type 2B

References:

Genes:

MONDO:0011570 - Charcot-Marie-Tooth disease type 2B2

References:

Genes:

MONDO:0011091 - Charcot-Marie-Tooth disease type 2D

References:

Genes:

MONDO:0014735 - Charcot-Marie-Tooth disease type 2Y

References:

Genes:

MONDO:0011066 - Charcot-Marie-Tooth disease type 4B1

References:

Genes:

MONDO:0011534 - Charcot-Marie-Tooth disease type 4G

References:

Genes:

MONDO:0012640 - Charcot-Marie-Tooth disease type 4J

References:

Genes:

MONDO:0014733 - Charcot-Marie-Tooth disease type 4K

References:

Genes:

MONDO:0010479 - Charcot-Marie-Tooth disease X-linked dominant 6

References:

Genes:

MONDO:0010689 - Charcot-Marie-Tooth disease X-linked recessive 4

References:

Genes:

MONDO:0010699 - Charcot-Marie-Tooth disease X-linked recessive 5

References:

Genes:

MONDO:0014906 - Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;

References:

Genes:

MONDO:0032728 - Charcot-Marie-Tooth disease, axonal, type 2EE

References:

Genes:

MONDO:0011675 - Charcot-Marie-Tooth Disease, axonal, type 2GG

References:

Genes:

MONDO:0980969 - Charcot-Marie-Tooth disease, axonal, type 2LL

References:

Genes:

MONDO:0980971 - charcot-marie-tooth disease, axonal, type 2MM

References:

Genes:

MONDO:0030677 - Charcot-Marie-Tooth disease, demyelinating, IIA 1I

References:

Genes:

MONDO:0008963 - Chediak-Higashi syndrome

References:

Genes:

MONDO:0018151 - coenzyme Q10 deficiency

References:

Genes:

MONDO:0011829 - coenzyme Q10 deficiency, primary, 1

References:

Genes:

MONDO:0013838 - coenzyme Q10 deficiency, primary, 3

References:

Genes:

MONDO:0033615 - coenzyme q10 deficiency, primary, 9

References:

Genes:

MONDO:0013837 - deafness-encephaloneuropathy-obesity-valvulopathy syndrome

References:

Genes:

MONDO:0013840 - encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome

References:

Genes:

MONDO:0007100 - familial amyloid neuropathy

References:

Genes:

MONDO:0013836 - familial steroid-resistant nephrotic syndrome with sensorineural deafness

References:

Genes:

MONDO:0011730 - fumaric aciduria

References:

Genes:

MONDO:0009748 - hereditary sensory and autonomic neuropathy with spastic paraplegia

References:

Genes:

MONDO:0013584 - hereditary sensory neuropathy-deafness-dementia syndrome

References:

Genes:

MONDO:0010043 - hereditary spastic paraplegia 17

References:

Genes:

MONDO:0009353 - homocystinuria due to methylene tetrahydrofolate reductase deficiency

References:

Genes:

MONDO:0009723 - Leigh syndrome

References:

Genes:

MONDO:0013762 - lipoic acid synthetase deficiency

References:

Genes:

MONDO:0014025 - lower motor neuron syndrome with late-adult onset

References:

Genes:

MONDO:0016814 - maternally-inherited Leigh syndrome

References:

Genes:

MONDO:0018868 - metachromatic leukodystrophy

References:

Genes:

MONDO:0010184 - methylmalonic aciduria and homocystinuria type cblC

References:

Genes:

MONDO:0008758 - mitochondrial DNA depletion syndrome 4a

References:

Genes:

MONDO:0013350 - mitochondrial DNA depletion syndrome 4b

References:

Genes:

MONDO:0012792 - mitochondrial DNA depletion syndrome 8a

References:

Genes:

MONDO:0976133 - myopathy, myofibrillar, 13, with rimmed vacuoles

References:

Genes:

MONDO:0014562 - neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

References:

Genes:

MONDO:0971150 - neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity

References:

Genes:

MONDO:0030055 - neuronopathy, distal hereditary motor, autosomal recessive 8

References:

Genes:

MONDO:0957874 - neuronopathy, distal hereditary motor, autosomal recessive 9

References:

Genes:

MONDO:0008025 - neuronopathy, distal hereditary motor, type 2A

References:

Genes:

MONDO:0012080 - neuronopathy, distal hereditary motor, type 2B

References:

Genes:

MONDO:0013243 - neuronopathy, distal hereditary motor, type 2C

References:

Genes:

MONDO:0015353 - neuronopathy, distal hereditary motor, type 5A

References:

Genes:

MONDO:0013884 - neuronopathy, distal hereditary motor, type 5B

References:

Genes:

MONDO:0030860 - neuronopathy, distal hereditary motor, type 5C

References:

Genes:

MONDO:0011879 - neuronopathy, distal hereditary motor, type 7B

References:

Genes:

MONDO:0060585 - neuronopathy, distal hereditary motor, type 9

References:

Genes:

MONDO:0011002 - neuropathy, hereditary motor and sensory, type 6A

References:

Genes:

MONDO:0032792 - neuropathy, hereditary motor and sensory, type VIc, with optic atrophy

References:

Genes:

MONDO:0008086 - neuropathy, hereditary sensory and autonomic, type 1A

References:

Genes:

MONDO:0013337 - neuropathy, hereditary sensory and autonomic, type 1C

References:

Genes:

MONDO:0013634 - neuropathy, hereditary sensory, type 2C

References:

Genes:

MONDO:0011871 - Niemann-Pick disease type B

References:

Genes:

MONDO:0009796 - ornithine aminotransferase deficiency

References:

Genes:

MONDO:0008759 - oxoglutaricaciduria

References:

Genes:

MONDO:0013948 - peroxisome biogenesis disorder 10A (Zellweger)

References:

Genes:

MONDO:0054549 - peroxisome biogenesis disorder 10B

References:

Genes:

MONDO:0013949 - peroxisome biogenesis disorder 11A (Zellweger)

References:

Genes:

MONDO:0013950 - peroxisome biogenesis disorder 11B

References:

Genes:

MONDO:0013951 - peroxisome biogenesis disorder 12A (Zellweger)

References:

Genes:

MONDO:0013952 - peroxisome biogenesis disorder 13A (Zellweger)

References:

Genes:

MONDO:0013967 - peroxisome biogenesis disorder 14B

References:

Genes:

MONDO:0008953 - peroxisome biogenesis disorder 1A (Zellweger)

References:

Genes:

MONDO:0011101 - peroxisome biogenesis disorder 1B

References:

Genes:

MONDO:0008954 - peroxisome biogenesis disorder 2A (Zellweger)

References:

Genes:

MONDO:0008736 - peroxisome biogenesis disorder 2B

References:

Genes:

MONDO:0013927 - peroxisome biogenesis disorder 3A (Zellweger)

References:

Genes:

MONDO:0013930 - peroxisome biogenesis disorder 4A (Zellweger)

References:

Genes:

MONDO:0013931 - peroxisome biogenesis disorder 4B

References:

Genes:

MONDO:0013936 - peroxisome biogenesis disorder 6A (Zellweger)

References:

Genes:

MONDO:0013937 - peroxisome biogenesis disorder 6B

References:

Genes:

MONDO:0013938 - peroxisome biogenesis disorder 7A (Zellweger)

References:

Genes:

MONDO:0013939 - peroxisome biogenesis disorder 7B

References:

Genes:

MONDO:0013942 - peroxisome biogenesis disorder 8A (Zellweger)

References:

Genes:

MONDO:0013943 - peroxisome biogenesis disorder 8B

References:

Genes:

MONDO:0013945 - peroxisome biogenesis disorder 9B

References:

Genes:

MONDO:0100259 - peroxisome biogenesis disorder due to PEX1 defect

References:

Genes:

MONDO:0100263 - peroxisome biogenesis disorder due to PEX6 defect

References:

Genes:

MONDO:0009959 - peroxisome biogenesis disorder type 3B

References:

Genes:

MONDO:0014754 - primary coenzyme Q10 deficiency 8

References:

Genes:

MONDO:0013382 - progressive demyelinating neuropathy with bilateral striatal necrosis

References:

Genes:

MONDO:0019169 - pyruvate dehydrogenase deficiency

References:

Genes:

MONDO:0010717 - pyruvate dehydrogenase E1-alpha deficiency

References:

Genes:

MONDO:0013580 - pyruvate dehydrogenase E1-beta deficiency

References:

Genes:

MONDO:0009502 - pyruvate dehydrogenase E2 deficiency

References:

Genes:

MONDO:0009529 - pyruvate dehydrogenase E3 deficiency

References:

Genes:

MONDO:0009503 - pyruvate dehydrogenase E3-binding protein deficiency

References:

Genes:

MONDO:0012120 - pyruvate dehydrogenase phosphatase deficiency

References:

Genes:

MONDO:0008972 - rhizomelic chondrodysplasia punctata type 1

References:

Genes:

MONDO:0014743 - rhizomelic chondrodysplasia punctata type 5

References:

Genes:

MONDO:0011835 - sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

References:

Genes:

MONDO:0859279 - spinal muscular atrophy, distal, autosomal recessive, 6

References:

Genes:

MONDO:0009669 - spinal muscular atrophy, type 1

References:

Genes:

MONDO:0009673 - spinal muscular atrophy, type II

References:

Genes:

MONDO:0009672 - spinal muscular atrophy, type III

References:

Genes:

MONDO:0010056 - spinal muscular atrophy, type IV

References:

Genes:

MONDO:0011801 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1

References:

Genes:

MONDO:0018996 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

References:

Genes:

MONDO:0008695 - VPS13A-related neurodegenerative disease

References:

Genes:

MONDO:0010338 - X-linked distal spinal muscular atrophy type 3

References:

Genes:

MONDO:0010378 - X-linked hereditary sensory and autonomic neuropathy with hearing loss

References:

Genes:

MONDO:0019609 - Zellweger spectrum disorders

References:

Genes: