PomBase home

Disease association ontology term - MONDO:0003620 - peripheral nervous system disorder

Term summary

ID
MONDO:0003620
Name
peripheral nervous system disorder
Ontology or CV name
Disease association
Definition
A disease involving the peripheral nervous system.

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:0004183 - axonal neuropathy

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:0011444 - Duane retraction syndrome 2

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:0000448 - paraganglioma

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:0008192 - pheochromocytoma/paraganglioma syndrome 1

References:

Genes:

MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2

References:

Genes:

MONDO:0011544 - pheochromocytoma/paraganglioma syndrome 3

References:

Genes:

MONDO:0007273 - pheochromocytoma/paraganglioma syndrome 4

References:

Genes:

MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5

References:

Genes:

MONDO:0032771 - pheochromocytoma/paraganglioma syndrome 7

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:0024517 - SMARCB1-related schwannomatosis

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:0019609 - Zellweger spectrum disorders

References:

Genes: