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"

4 matching diseasesClear search ×

Isolated glycerol kinase deficiency

Hyperglycerolemia

ORPHA:408

Glycine encephalopathy

NKA · Non-ketotic hyperglycinemia

ORPHA:407

Propionic acidemia

Ketotic hyperglycinemia · Propionic aciduria

ORPHA:35

Rare hypercholesterolemia

ORPHA:477811