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"

2 matching diseasesClear search ×

Mucolipidosis type III alpha/beta

ML 3 alpha/beta · ML III alpha/beta

ORPHA:423461

Mucolipidosis type II

I-cell disease · N-acetylglucosamine 1-phosphotransferase deficiency

ORPHA:576