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 ×

Hartnup disease

Aminoaciduria, Hartnup type · Hartnup disorder

ORPHA:2116

Dicarboxylic aminoaciduria

Glutamate-aspartate transport defect

ORPHA:2195

Lysinuric protein intolerance

LPI · Hyperdibasic aminoaciduria

ORPHA:470

OBSOLETE: Hyperdibasic aminoaciduria type 1

ORPHA:1032