EMG: neuropathic changes
Symptom Information:
Symptom ID: | HPO:0003445 | |||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) EMG abnormality(HPO:0003457) EMG: neuropathic changes(HPO:0003445) MedDRA: |
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Database Frequency: | 21 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Adult-onset proximal spinal muscular atrophy, autosomal dominant | (Orphanet:209335) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | (Orphanet:209341) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Distal hereditary motor neuropathy type 2 | (Orphanet:139525) |
Distal spinal muscular atrophy type 3 | (Orphanet:139547) |
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY | (OMIM:606183) |
Laing distal myopathy | (Orphanet:59135) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MUSCLE CRAMPS, FAMILIAL | (OMIM:158400) |
Monomelic amyotrophy | (Orphanet:65684) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB | (OMIM:608634) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
Nemaline myopathy | (Orphanet:607) |
Pontocerebellar hypoplasia type 1 | (Orphanet:2254) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Proximal spinal muscular atrophy type 4 | (Orphanet:83420) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
X-linked distal spinal muscular atrophy | (Orphanet:139557) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |