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PGM3-CDG

Disease Summary
Associated Targets (3)
Tdark

2

Tbio

1


GARD Rare
Uniprot Description A primary immunodeficiency syndrome characterized by recurrent respiratory and skin infections beginning in early childhood, severe atopy, increased serum IgE, and developmental delay or cognitive impairment of varying severity.
Mondo Term and Equivalent IDs
MONDO:0014353:  PGM3-CDG
GARD:0004331: 
Orphanet:443811: 
UMLS:C4014371: