Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

5 matching diseasesClear search ×

Leukocyte adhesion deficiency type III

LAD-1 variant · LAD-III

ORPHA:99844

Infantile LAD-like disease due to RAC2 deficiency

Infantile leukocyte adhesion deficiency due to Rac family small GTPase 2 deficiency

ORPHA:183707

Leukocyte adhesion deficiency

LAD

ORPHA:2968

Leukocyte adhesion deficiency type I

LAD-I

ORPHA:99842

Leukocyte adhesion deficiency type II

CDG syndrome type IIc · CDG-IIc

ORPHA:99843