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 ×

Metabolic myopathy due to lactate transporter defect

Erythrocyte lactate transporter defect

ORPHA:171690

Dicarboxylic aminoaciduria

Glutamate-aspartate transport defect

ORPHA:2195

Systemic primary carnitine deficiency

CDSP · CUD

ORPHA:158