Abnormality of peripheral nerve conduction

Symptom Information:

Symptom ID: HPO:0003134
Synonyms:
Sensory and motor nerve conduction abnormalities [HPO:0003134]
Nerve conduction abnormality [Orphanet:43130]
Abnormal nerve conduction (finding) [Orphanet:43130]
Abnormal nerve conduction [Orphanet:43130]
Quality:
Cross references:
Orphanet:43130 "Nerve conduction abnormality" [Orphanet:43130]
UMLS:C0234090 "Abnormal nerve conduction" [Orphanet:43130]
Is a (Direct Parents):
Orphanet Decreased nerve conduction velocity
Orphanet Functional anomalies of the nervous system
HPO         Abnormal nerve conduction velocity
HPO         Abnormal peripheral nervous system morphology
HPO         Abnormal peripheral action potential amplitude
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:
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)