EMG: neuropathic changes

Symptom Information:

Symptom ID: HPO:0003445
Synonyms:
EMG: neurogenic abnormalities [HPO:0003445]
EMG: neurogenic changes [HPO:0003445]
EMG: neurogenic findings [HPO:0003445]
Quality:
Cross references:
Is a (Direct Parents):
HPO         EMG abnormality
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:
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)