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"

8 matching diseasesClear search ×

OBSOLETE: Combined hyperlipidemia

OBSOLETE: Mixed hyperlipidemia · OBSOLETE: Mixed hyperlipoproteinemia

ORPHA:79211

Dysbetalipoproteinemia

Remnant hyperlipoproteinemia · HLP type 3

ORPHA:412

Familial Hyperalphalipoproteinemia

ORPHA:181428

Hyperlipoproteinemia type 1

HLP type 1

ORPHA:411

Hypoalphalipoproteinemia

ORPHA:31153

Hypobetalipoproteinemia

ORPHA:31154

OBSOLETE: Cholesterol-ester transfer protein deficiency

OBSOLETE: CEPT deficiency · OBSOLETE: Familial hyperalphalipoproteinemia type I

ORPHA:79506

OBSOLETE: Hyperlipoproteinemia type 5

OBSOLETE: HLP type 5 · OBSOLETE: Major hyperlipidemia

ORPHA:70470