Peripheral neuropathy

Symptom Information:

Symptom ID: HPO:0009830
Synonyms:
Neuropathy [HPO:0009830]
Peripheral nerve disease (disorder) [Orphanet:43060]
Peripheral Neuropathy [Orphanet:43060]
Neuropathy [OMIM:Neuropathy]
Peripheral neuropathy [OMIM:Peripheral neuropathy]
Peripheral neuropathy [Orphanet:43060]
Neuropathy peripheral [Orphanet:43060]
Neuropathy peripheral [MedDRA:10029331]
Hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Hereditary and idiopathic peripheral neuropathy, other [MedDRA:10029331]
Inflammatory and toxic neuropathy [MedDRA:10029331]
Neuritis peripheral [MedDRA:10029331]
Neuropathy [MedDRA:10029331]
Neuropathy - (NOS) [MedDRA:10029331]
Neuropathy NOS [MedDRA:10029331]
Other hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Other inflammatory and toxic neuropathies [MedDRA:10029331]
Other specified idiopathic peripheral neuropathy [MedDRA:10029331]
Peripheral neuritis [MedDRA:10029331]
Peripheral neuritis antepartum [MedDRA:10029331]
Peripheral neuritis in pregnancy [MedDRA:10029331]
Peripheral neuritis in pregnancy, unspecified as to episode of care [MedDRA:10029331]
Peripheral neuritis in pregnancy, with delivery [MedDRA:10029331]
Peripheral neuritis in pregnancy, with delivery, with mention of postpartum complication [MedDRA:10029331]
Peripheral neuritis NOS [MedDRA:10029331]
Peripheral neuritis postartum [MedDRA:10029331]
Peripheral neuropathy aggravated [MedDRA:10029331]
Peripheral neuropathy NOS [MedDRA:10029331]
Unspecified hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Unspecified idiopathic peripheral neuropathy [MedDRA:10029331]
Unspecified inflammatory and toxic neuropathies [MedDRA:10029331]
Peripheral nerve disorder NOS [MedDRA:10029331]
Peripheral neuritis postpartum [MedDRA:10029331]
Cold sensitivity neuropathy [MedDRA:10029331]
Neuropathy (motor and sensory) [OMIM:Neuropathy (motor and sensory)]
No peripheral neuropathy [OMIM:No peripheral neuropathy]
Peripheral neuritis [OMIM:Peripheral neuritis]
Peripheral neuropathy (1 patient) [OMIM:Peripheral neuropathy (1 patient)]
Peripheral neuropathy (in some patients) [OMIM:Peripheral neuropathy (in some patients)]
Peripheral neuropathy (reported in 1 patient) [OMIM:Peripheral neuropathy (reported in 1 patient)]
Peripheral neuropathy (some patients) [OMIM:Peripheral neuropathy (some patients)]
Peripheral neuropathy (variable) [OMIM:Peripheral neuropathy (variable)]
Polyneuritis [MedDRA:10036104]
Neuritis (disorder) [Orphanet:43070]
Peripheral neuritis (disorder) [Orphanet:43070]
Polyneuritis (disorder) [Orphanet:43070]
Polyneuritis [Orphanet:43070]
Neuritis [Orphanet:43070]
Neuritis/polyneuritis/multineuritis [Orphanet:43070]
Polyneuritis [OMIM:Polyneuritis]
Neuritis [MedDRA:10029240]
Peripheral neuropathies [MedDRA:10034606]
Quality:
Cross references:
HPO:0003477 "Peripheral axonal neuropathy" [Orphanet:43060]
HPO:0007178 "Motor polyneuropathy" [Orphanet:43060]
Orphanet:43060 "Peripheral neuropathy" [Orphanet:43060]
Orphanet:43070 "Neuritis/polyneuritis/multineuritis" [Orphanet:43070]
OMIM: "Neuropathy" [OMIM:Neuropathy]
OMIM: "Peripheral neuropathy" [OMIM:Peripheral neuropathy]
OMIM: "Neuropathy (motor and sensory)" [OMIM:Neuropathy (motor and sensory)]
OMIM: "No peripheral neuropathy" [OMIM:No peripheral neuropathy]
OMIM: "Peripheral neuritis" [OMIM:Peripheral neuritis]
OMIM: "Peripheral neuropathy (1 patient)" [OMIM:Peripheral neuropathy (1 patient)]
OMIM: "Peripheral neuropathy (in some patients)" [OMIM:Peripheral neuropathy (in some patients)]
OMIM: "Peripheral neuropathy (reported in 1 patient)" [OMIM:Peripheral neuropathy (reported in 1 patient)]
OMIM: "Peripheral neuropathy (some patients)" [OMIM:Peripheral neuropathy (some patients)]
OMIM: "Peripheral neuropathy (variable)" [OMIM:Peripheral neuropathy (variable)]
OMIM: "Polyneuritis" [OMIM:Polyneuritis]
UMLS:C0031117 "Peripheral Neuropathy" [Orphanet:43060]
UMLS:C0032541 "Polyneuritis" [Orphanet:43070]
UMLS:C0027813 "Neuritis" [Orphanet:43070]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
HPO         Abnormal peripheral nervous system morphology
Orphanet Peripheral axonal neuropathy
MedDRA Peripheral neuropathies NEC
MedDRA Nervous system disorders
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)
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)