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 ×

Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency

ALPS due to CTLA4 haploinsuffiency · CHAI

ORPHA:436159

Immune dysregulation disease with immunodeficiency

ORPHA:169361

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590