Hypoglycosylation of alpha-dystroglycan

Symptom Information:

Symptom ID: HPO:0030046
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource: HPO

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
DPM3-CDG (Orphanet:263494)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 (OMIM:616052)