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 ×

Blomstrand lethal chondrodysplasia

BLC · BOCD

ORPHA:50945

Pseudo-TORCH syndrome type 1

Band like calcification with simplified gyration and polymicrogyria · BLC-PMG

ORPHA:1229

Methylmalonic acidemia with homocystinuria, type cblC

CblC defect · Cobalamin C defect

ORPHA:79282