Polyneuropathy
Symptom Information:
Symptom ID: | HPO:0001271 | |||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |