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"

5 matching diseasesClear search ×

Neutral lipid storage disease

Lipidosis with triglyceride storage disease

ORPHA:165

Glycogen storage disease

GSD · Glycogenosis

ORPHA:79201

Lipid storage disease

ORPHA:79204

Neutral lipid storage disease with ichthyosis

NLSDI · Dorfman-Chanarin syndrome

ORPHA:98907

Neutral lipid storage disease with myopathy

Neutral lipid storage disease type M · NLSDM

ORPHA:98908