Hypoalphalipoproteinemia, Primary, 1 (FHA1)

Hypoalphalipoproteinemia, Primary, 1(来自ICD-11)

别称:

Familial Hypoalphalipoproteinemia

Familial Hdl Deficiency

Fha

High Density Lipoprotein Deficiency

Primary Hypoalphalipoproteinemia 1

Hdl Deficiency, Type 2

Hdld

Fhd

High Density Lipoprotein Deficiency 2

Hypoalphalipoproteinemia, Familial

Familial Hypoalphalipo-Proteinemia

Primary Hypoalphalipoproteinemia

Hdl Deficiency, Familial, 1

Hdl Cholesterol, Low Serum

Low Serum Hdl Cholesterol

Hypoalphalipoproteinemia

Hdld2

Hdlc

Fha1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hypoalphalipoproteinemia, Primary, 1, also known as familial hypoalphalipoproteinemia, is related to abdominal obesity-metabolic syndrome 1 and fish-eye disease. An important gene associated with Hypoalphalipoproteinemia, Primary, 1 is ABCA1 (ATP Binding Cassette Subfamily A Member 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and ESR-mediated signaling. The drugs Niacin and Nicotinamide have been mentioned in the context of this disorder. Affiliated tissues include liver and heart, and related phenotypes are premature coronary artery atherosclerosis and hypertriglyceridemia

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