Abnormal N-glycosylation of transferrin

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Abnormal N-glycosylation of transferrin" [OMIM:Abnormal N-glycosylation of transferrin]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Congenital muscular dystrophy with intellectual disability and severe epilepsy (Orphanet:329178)