Decreased nerve conduction velocity
Symptom Information:
Symptom ID: | HPO:0000762 | |||||||||||||||||||||
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) MedDRA: |
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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) |