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"

3 matching diseasesClear search ×

Leukocyte adhesion deficiency type III

LAD-1 variant · LAD-III

ORPHA:99844

Mild phenylketonuria

Mild PKU · mPKU

ORPHA:79253

Variant of Guillain-Barré syndrome

Variant of GBS

ORPHA:231413