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 ×

Macrocephaly-spastic paraplegia-dysmorphism syndrome

Fryns macrocephaly

ORPHA:2429

Autosomal recessive primary microcephaly

MCPH · Microcephalia vera

ORPHA:2512