Abnormality of peripheral nerve conduction
Symptom Information:
Symptom ID: | HPO:0003134 | ||||
Synonyms: |
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Cross references: |
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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) Abnormality of peripheral nerve conduction(HPO:0003134) MedDRA: |
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Database Frequency: | 38 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acromicric dysplasia | (Orphanet:969) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
CEDNIK syndrome | (Orphanet:66631) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cataract - ataxia - deafness | (Orphanet:1368) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Cockayne syndrome | (Orphanet:191) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Friedreich ataxia 2 | (OMIM:601992) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Infantile axonal neuropathy | (Orphanet:2679) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
MELAS | (Orphanet:550) |
Metachromatic leukodystrophy | (Orphanet:512) |
Methylcobalamin deficiency type cblE | (Orphanet:2169) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Monomelic amyotrophy | (Orphanet:65684) |
Multiple sulfatase deficiency | (Orphanet:585) |
POEMS syndrome | (Orphanet:2905) |
Perrault Syndrome | (Orphanet:2855) |
Polyneuropathy - hand defect | (Orphanet:2926) |
Polyneuropathy - intellectual deficit - acromicria - premature menopause | (Orphanet:2928) |
Roussy-Lévy syndrome | (Orphanet:3115) |
Scheie syndrome | (Orphanet:93474) |
Scleroderma | (Orphanet:801) |
Sialidosis type 1 | (Orphanet:812) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |
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 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |