Defect in N- and O-glycosylation

Symptom Information:

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

All diseases associated with this symptom:

Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)