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 II

CDG syndrome type IIc · CDG-IIc

ORPHA:99843

Leukocyte adhesion deficiency type III

LAD-1 variant · LAD-III

ORPHA:99844

Laryngotracheoesophageal cleft type 2

Laryngo-tracheo-esophageal cleft type 2 · LTEC II

ORPHA:93939

Leukocyte adhesion deficiency

LAD

ORPHA:2968

Leukocyte adhesion deficiency type I

LAD-I

ORPHA:99842