[DEL]Myopathic changes seen on EMG

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
HPO:0003458 EMG: myopathic abnormalities [du]
Quality:
Cross references:
OMIM: "Myopathic changes seen on EMG" [OMIM:Myopathic changes seen on EMG]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Muscular dystrophy, Selcen type (Orphanet:199340)