Rare Disease Library

Apolipoprotein A-I deficiency

ApoA-I deficiency · Familial apoA-I deficiency

Abetalipoproteinemia

Bassen-Kornzweig disease · Homozygous familial hypobetalipoproteinemia

Dysbetalipoproteinemia

Remnant hyperlipoproteinemia · HLP type 3

Familial Hyperalphalipoproteinemia

Familial hypercholanemia

Hereditary hypercholanemia

Familial hyperinsulinism

FHI · Familial hyperinsulinemic hypoglycemia

Familial hyperprolactinemia

Familial isolated prolactin receptor deficiency

Familial hypodysfibrinogenemia

Familial hypofibrinogenemia

Hereditary renal hypouricemia

Familial renal hypouricemia

Hyperlipoproteinemia type 1

HLP type 1

Hypoalphalipoproteinemia

Hypobetalipoproteinemia

OBSOLETE: Cholesterol-ester transfer protein deficiency

OBSOLETE: CEPT deficiency · OBSOLETE: Familial hyperalphalipoproteinemia type I

Tangier disease

ATP-binding cassette transporter A1 deficiency · Analphalipoproteinemia