Decreased nerve conduction velocity

Symptom Information:

Symptom ID: HPO:0000762
Synonyms:
Abnormal nerve conduction [HPO:0000762]
Decreased nerve conduction velocities (NCV) [HPO:0000762]
Delayed nerve conduction velocity [HPO:0000762]
Nerve conduction abnormalities [HPO:0000762]
Reduced nerve conduction velocities [HPO:0000762]
Slow nerve conduction velocity [HPO:0000762]
Slowed nerve conduction velocities [HPO:0000762]
Somatosensory evoked potential anomaly [Orphanet:43130]
Decreased nerve conduction velocities (NCV) [OMIM:Decreased nerve conduction velocities (NCV)]
Decreased nerve conduction velocity [OMIM:Decreased nerve conduction velocity]
Delayed nerve conduction velocity [OMIM:Delayed nerve conduction velocity]
Nerve conduction abnormalities [OMIM:Nerve conduction abnormalities]
Reduced nerve conduction velocities [OMIM:Reduced nerve conduction velocities]
Slow nerve conduction velocity [OMIM:Slow nerve conduction velocity]
Slowed nerve conduction velocities [OMIM:Slowed nerve conduction velocities]
Nerve conduction abnormality [Orphanet:43130]
Decreased nerve conduction velocities [OMIM:Decreased nerve conduction velocities]
Decreased nerve conduction velocities (NCV) (30%) [OMIM:Decreased nerve conduction velocities (NCV) (30%)]
Nerve conduction velocity (NCV) slowing [OMIM:Nerve conduction velocity (NCV) slowing]
Reduced nerve conduction velocities (demyelinating range) [OMIM:Reduced nerve conduction velocities (demyelinating range)]
Slowed nerve conduction velocities (NCV) [OMIM:Slowed nerve conduction velocities (NCV)]
Quality:
Cross references:
Orphanet:43130 "Nerve conduction abnormality" [Orphanet:43130]
OMIM: "Decreased nerve conduction velocities (NCV)" [OMIM:Decreased nerve conduction velocities (NCV)]
OMIM: "Decreased nerve conduction velocity" [OMIM:Decreased nerve conduction velocity]
OMIM: "Delayed nerve conduction velocity" [OMIM:Delayed nerve conduction velocity]
OMIM: "Nerve conduction abnormalities" [OMIM:Nerve conduction abnormalities]
OMIM: "Reduced nerve conduction velocities" [OMIM:Reduced nerve conduction velocities]
OMIM: "Slow nerve conduction velocity" [OMIM:Slow nerve conduction velocity]
OMIM: "Slowed nerve conduction velocities" [OMIM:Slowed nerve conduction velocities]
OMIM: "Decreased nerve conduction velocities" [OMIM:Decreased nerve conduction velocities]
OMIM: "Decreased nerve conduction velocities (NCV) (30%)" [OMIM:Decreased nerve conduction velocities (NCV) (30%)]
OMIM: "Nerve conduction velocity (NCV) slowing" [OMIM:Nerve conduction velocity (NCV) slowing]
OMIM: "Reduced nerve conduction velocities (demyelinating range)" [OMIM:Reduced nerve conduction velocities (demyelinating range)]
OMIM: "Slowed nerve conduction velocities (NCV)" [OMIM:Slowed nerve conduction velocities (NCV)]
Is a (Direct Parents):
HPO         Abnormality of peripheral nerve conduction
Orphanet Functional anomalies of the nervous system
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)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Ataxia - pancytopenia (Orphanet:2585)
Autosomal dominant slowed nerve conduction velocity (Orphanet:140481)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Bifunctional enzyme deficiency (Orphanet:300)
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Charcot-Marie-Tooth disease type 4B3 (Orphanet:363981)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Charcot-Marie-Tooth disease type 4G (Orphanet:99953)
Charcot-Marie-Tooth disease type 4J (Orphanet:139515)
Chédiak-Higashi syndrome (Orphanet:167)
Cockayne syndrome (Orphanet:191)
Combined oxidative phosphorylation defect type 13 (Orphanet:319514)
Distal myopathy with vocal cord weakness (Orphanet:600)
Fetal akinesia-cerebral and retinal hemorrhage syndrome (Orphanet:363409)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Infantile neuroaxonal dystrophy (Orphanet:35069)
KRABBE DISEASE (OMIM:245200)
Krabbe disease (Orphanet:487)
MELAS (Orphanet:550)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY (OMIM:249900)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600)
NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE (OMIM:162600)
Navajo neurohepatopathy (Orphanet:255229)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract (Orphanet:171848)
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY (OMIM:183050)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Spinocerebellar ataxia type 10 (Orphanet:98761)
X-linked Charcot-Marie-Tooth disease type 3 (Orphanet:101077)
Xeroderma pigmentosum complementation group B (Orphanet:276252)