Carbohydrate moiety deficiency of secretory glycoproteins, lysosomal enzymes, and probably membrane glycoproteins

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Carbohydrate moiety deficiency of secretory glycoproteins, lysosomal enzymes, and probably membrane glycoproteins" [OMIM:Carbohydrate moiety deficiency of secretory glycoproteins, lysosomal enzymes, and probably membrane glycoproteins]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx (OMIM:212067)