Decreased motor nerve conduction velocity

Symptom Information:

Symptom ID: HPO:0003431
Synonyms:
Decreased motor nerve conduction velocities (NCV) [HPO:0003431]
Decreased motor nerve conduction velocity (NCV) [HPO:0003431]
Reduced motor nerve conduction velocity [HPO:0003431]
Decreased motor nerve conduction velocities (NCV) [OMIM:Decreased motor nerve conduction velocities (NCV)]
Decreased motor nerve conduction velocity (NCV) [OMIM:Decreased motor nerve conduction velocity (NCV)]
Reduced motor nerve conduction velocity [OMIM:Reduced motor nerve conduction velocity]
Decreased motor nerve conduction velocities [OMIM:Decreased motor nerve conduction velocities]
Decreased motor nerve conduction velocity (NCV) (15-30 m/s) [OMIM:Decreased motor nerve conduction velocity (NCV) (15-30 m/s)]
Decreased motor nerve conduction velocity (NCV) (less than 20 m/s) [OMIM:Decreased motor nerve conduction velocity (NCV) (less than 20 m/s)]
Decreased motor nerve conduction velocity (NCV) (less than 38 m/s) [OMIM:Decreased motor nerve conduction velocity (NCV) (less than 38 m/s)]
Decreased motor nerve conduction velocity (in some patients) [OMIM:Decreased motor nerve conduction velocity (in some patients)]
Reduced motor nerve conduction velocity (NCV) (range less than 38 m/s to normal) [OMIM:Reduced motor nerve conduction velocity (NCV) (range less than 38 m/s to normal)]
Quality:
Cross references:
OMIM: "Decreased motor nerve conduction velocities (NCV)" [OMIM:Decreased motor nerve conduction velocities (NCV)]
OMIM: "Decreased motor nerve conduction velocity (NCV)" [OMIM:Decreased motor nerve conduction velocity (NCV)]
OMIM: "Reduced motor nerve conduction velocity" [OMIM:Reduced motor nerve conduction velocity]
OMIM: "Decreased motor nerve conduction velocities" [OMIM:Decreased motor nerve conduction velocities]
OMIM: "Decreased motor nerve conduction velocity (NCV) (15-30 m/s)" [OMIM:Decreased motor nerve conduction velocity (NCV) (15-30 m/s)]
OMIM: "Decreased motor nerve conduction velocity (NCV) (less than 20 m/s)" [OMIM:Decreased motor nerve conduction velocity (NCV) (less than 20 m/s)]
OMIM: "Decreased motor nerve conduction velocity (NCV) (less than 38 m/s)" [OMIM:Decreased motor nerve conduction velocity (NCV) (less than 38 m/s)]
OMIM: "Decreased motor nerve conduction velocity (in some patients)" [OMIM:Decreased motor nerve conduction velocity (in some patients)]
OMIM: "Reduced motor nerve conduction velocity (NCV) (range less than 38 m/s to normal)" [OMIM:Reduced motor nerve conduction velocity (NCV) (range less than 38 m/s to normal)]
Is a (Direct Parents):
HPO         Decreased nerve conduction velocity
HPO         Abnormal motor neuron morphology
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:
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)