Peripheral neuropathy
Symptom Information:
Symptom ID: | HPO:0009830 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) MedDRA: Nervous system disorders(MedDRA:10029205) Peripheral neuropathy(HPO:0009830) Peripheral axonal neuropathy(HPO:0003477) Peripheral neuropathies NEC(MedDRA:10034607) Peripheral neuropathy(HPO:0009830) |
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Database Frequency: | 206 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1 | (OMIM:105250) |
ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA | (OMIM:208700) |
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
ATAXIA-OCULOMOTOR APRAXIA 4 | (OMIM:616267) |
Acrodysostosis | (Orphanet:950) |
Acroosteolysis, dominant type | (Orphanet:955) |
Adiposis dolorosa | (Orphanet:36397) |
Adult polyglucosan body disease | (Orphanet:206583) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alström syndrome | (Orphanet:64) |
Argininemia | (Orphanet:90) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Attenuated Chédiak-Higashi syndrome | (Orphanet:352723) |
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Autosomal recessive spastic paraplegia type 23 | (Orphanet:101003) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Behr syndrome | (Orphanet:1239) |
Behçet disease | (Orphanet:117) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
CADASIL | (Orphanet:136) |
CARPAL TUNNEL SYNDROME | (OMIM:115430) |
CEDNIK syndrome | (Orphanet:66631) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
CINCA syndrome | (Orphanet:1451) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COFS syndrome | (Orphanet:1466) |
CONGENITAL DISORDER OF DEGLYCOSYLATION | (OMIM:615273) |
CRANIAL NERVES, RECURRENT PARESIS OF | (OMIM:218200) |
Castleman disease | (Orphanet:160) |
Cataract - ataxia - deafness | (Orphanet:1368) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Charcot-Marie-Tooth disease - deafness - intellectual deficit | (Orphanet:90103) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Choreoacanthocytosis | (Orphanet:2388) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Chylomicron retention disease | (Orphanet:71) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cockayne syndrome | (Orphanet:191) |
Cogan syndrome | (Orphanet:1467) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
Congenital disorder of glycosylation | (Orphanet:137) |
Cornelia de Lange syndrome | (Orphanet:199) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE | (OMIM:124950) |
DEND syndrome | (Orphanet:79134) |
DYSAUTONOMIA-LIKE DISORDER | (OMIM:224000) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
Deafness - encephaloneuropathy - obesity - valvulopathy | (Orphanet:254898) |
Deafness - onychodystrophy | (Orphanet:3231) |
Disorder of bile acid synthesis | (Orphanet:79168) |
Distal hereditary motor neuropathy type 7 | (Orphanet:139589) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29 | (OMIM:616339) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erythromelalgia | (Orphanet:1956) |
Familial dysautonomia | (Orphanet:1764) |
Familial symmetric lipomatosis | (Orphanet:2398) |
Felty syndrome | (Orphanet:47612) |
Flynn-Aird syndrome | (Orphanet:2047) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Friedreich ataxia 1 | (OMIM:229300) |
Fucosidosis | (Orphanet:349) |
Gamma heavy-chain disease | (Orphanet:100026) |
Gamma-glutamylcysteine synthetase deficiency | (Orphanet:33574) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED | (OMIM:308200) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration | (Orphanet:85317) |
Kennedy disease | (Orphanet:481) |
Krabbe disease | (Orphanet:487) |
LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leber plus disease | (Orphanet:99718) |
Ledderhose disease | (Orphanet:199251) |
Legionellosis | (Orphanet:549) |
Leigh syndrome | (Orphanet:506) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
Leukoencephalopathy - dystonia - motor neuropathy | (Orphanet:163684) |
Lyme disease | (Orphanet:91546) |
MEDNIK syndrome | (Orphanet:171851) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MERRF | (Orphanet:551) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 | (OMIM:614053) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY | (OMIM:614741) |
Malignant atrophic papulosis | (Orphanet:679) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Maturity-onset diabetes of the young, type 2 | (OMIM:125851) |
Maturity-onset diabetes of the young, type 6 | (OMIM:606394) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Metachromatic leukodystrophy | (Orphanet:512) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Micro syndrome | (Orphanet:2510) |
Microscopic polyangiitis | (Orphanet:727) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Mixed connective tissue disease | (Orphanet:809) |
Muckle-Wells syndrome | (Orphanet:575) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |
NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY | (OMIM:256720) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB | (OMIM:608634) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA | (OMIM:608720) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC | (OMIM:614213) |
NEUROPATHY, PAINFUL | (OMIM:256870) |
NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE | (OMIM:162600) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurofibromatosis type 2 | (Orphanet:637) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Non-histaminic angioedema | (Orphanet:658) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Odontoleukodystrophy | (Orphanet:77295) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, ANDSPONGY DEGENERATION OF BRAIN | (OMIM:260970) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
PEROXISOME BIOGENESIS DISORDER 3B | (OMIM:266510) |
PMM2-CDG | (Orphanet:79318) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Pelizaeus-Merzbacher disease | (Orphanet:702) |
Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 1 | (OMIM:233400) |
Perrault Syndrome 5 | (OMIM:616138) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Porphyria variegata | (Orphanet:79473) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
Refsum disease | (Orphanet:773) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY | (OMIM:183050) |
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS | (OMIM:271322) |
Sarcoidosis | (Orphanet:797) |
Schnitzler syndrome | (Orphanet:37748) |
Scleroderma | (Orphanet:801) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Smith-Magenis syndrome | (Orphanet:819) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 8 | (Orphanet:98760) |
Stiff skin syndrome | (Orphanet:2833) |
Systemic sclerosis | (Orphanet:90291) |
Sézary syndrome | (Orphanet:3162) |
THALIDOMIDE SUSCEPTIBILITY | (OMIM:273600) |
Tangier disease | (Orphanet:31150) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Whipple disease | (Orphanet:3452) |
Wilson disease | (Orphanet:905) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
Wolfram syndrome | (Orphanet:3463) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
Xeroderma pigmentosum | (Orphanet:910) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |