Decreased motor nerve conduction velocity
Symptom Information:
Symptom ID: | HPO:0003431 | ||||||||||||
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) Abnormality of peripheral nerve conduction(HPO:0003134) Decreased nerve conduction velocity(HPO:0000762) Decreased motor nerve conduction velocity(HPO:0003431) Morphological abnormality of the central nervous system(HPO:0002011) Abnormal motor neuron morphology(HPO:0002450) Decreased motor nerve conduction velocity(HPO:0003431) MedDRA: |
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Database Frequency: | 51 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1C | (Orphanet:101083) |
Charcot-Marie-Tooth disease type 1D | (Orphanet:101084) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 1F | (Orphanet:101085) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 2B2 | (Orphanet:101101) |
Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
Charcot-Marie-Tooth disease type 4B1 | (Orphanet:99955) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEMATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS | (OMIM:601170) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB | (OMIM:614751) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |