Polyneuropathy

Symptom Information:

Symptom ID: HPO:0001271
Synonyms:
Polyneuropathy [OMIM:Polyneuropathy]
Polyneuropathy (98% of patients) [OMIM:Polyneuropathy (98% of patients)]
Quality:
Cross references:
OMIM: "Polyneuropathy" [OMIM:Polyneuropathy]
OMIM: "Polyneuropathy (98% of patients)" [OMIM:Polyneuropathy (98% of patients)]
UMLS:C0152025 "Polyneuropathy" [HPO:0001271]
Is a (Direct Parents):
HPO         Peripheral neuropathy
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)
                   Polyneuropathy(HPO:0001271)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

46,XY gonadal dysgenesis - motor and sensory neuropathy (Orphanet:168563)
APOLIPOPROTEIN A-I (OMIM:107680)
ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA (OMIM:208700)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
CEDNIK syndrome (Orphanet:66631)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
COCKAYNE SYNDROME A (OMIM:216400)
Cataract - ataxia - deafness (Orphanet:1368)
Cockayne syndrome (Orphanet:191)
Combined oxidative phosphorylation defect type 7 (Orphanet:254930)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial amyloidosis, Finnish type (Orphanet:85448)
Fucosidosis (Orphanet:349)
Gamma-glutamylcysteine synthetase deficiency (Orphanet:33574)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hypomyelination - congenital cataract (Orphanet:85163)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Leber plus disease (Orphanet:99718)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1 (OMIM:153600)
MELAS (Orphanet:550)
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY (OMIM:249900)
MONONEUROPATHY OF THE MEDIAN NERVE, MILD (OMIM:613353)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Myotilin-related myofibrillar myopathy without spheroid body (Orphanet:98911)
NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY (OMIM:256720)
PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, ANDSPONGY DEGENERATION OF BRAIN (OMIM:260970)
PEROXISOME BIOGENESIS DISORDER 14B (OMIM:614920)
PEROXISOME BIOGENESIS DISORDER 3B (OMIM:266510)
PMM2-CDG (Orphanet:79318)
Perrault Syndrome 1 (OMIM:233400)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polyneuropathy - hand defect (Orphanet:2926)
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract (Orphanet:171848)
Progressive demyelinating neuropathy with bilateral striatal necrosis (Orphanet:217396)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Ribose 5-phosphate isomerase deficiency (OMIM:608611)
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY (OMIM:183050)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS (OMIM:271322)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Spastic paraplegia type 2 (Orphanet:99015)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Tyrosinemia type 1 (Orphanet:882)
WERNICKE-KORSAKOFF SYNDROME (OMIM:277730)
Waardenburg-Shah syndrome (Orphanet:897)
Waldenström macroglobulinemia (Orphanet:33226)
Wilson disease (Orphanet:905)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
ZASP-related myofibrillar myopathy (Orphanet:98912)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)