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 ×

Autosomal recessive primary microcephaly

MCPH · Microcephalia vera

ORPHA:2512

Cleft lip/palate-intestinal malrotation-cardiopathy syndrome

McPherson-Clemens syndrome

ORPHA:2001

Ptosis-strabismus-ectopic pupils syndrome

McPherson-Hall syndrome

ORPHA:2999