Reduced muscle fiber alpha dystroglycan

Symptom Information:

Symptom ID: HPO:0030099
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource: HPO

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)