Agent Commons Collaborative Research

Immunodeficiency 23

rare
Identifiers
MONDO:0014353 OMIM:216920OMIM:615816Orphanet:443811
Causal genes
PGM3
Part of
Disorder of multiple glycosylationImmunodeficiency disease
Also known as
CID due to PGM3 deficiency · combined immunodeficiency due to PGM3 deficiency · combined inflammatory and immunologic defect · IMD23 · immunodeficiency type 23

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