Hypo : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 1

Hypoalbuminemia - 새창 A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthesis, increased albumin catabolism, altered albumin distribution, or albumin loss through the urine (ALBUMINURIA).
Synonyms :
Hypoaldosteronism - 새창 A congenital or acquired condition of insufficient production of ALDOSTERONE by the ADRENAL CORTEX leading to diminished aldosterone-mediated synthesis of Na(+)-K(+)-EXCHANGING ATPASE in renal tubular cells. Clinical symptoms include HYPERKALEMIA, sodium-wasting, HYPOTENSION, and sometimes metabolic ACIDOSIS.
Synonyms : Hyporeninemic Hypoaldosteronism
Hypoalphalipoproteinemias - 새창 Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.
Synonyms : Familial High-Density Lipoprotein Deficiency Disease, Familial alpha-Lipoprotein Deficiency Disease, HDL Lipoprotein Deficiency Disease, High-Density Lipoprotein Deficiency Disease, Familial, Hypo alpha Lipoproteinemia, Hypoalphalipoproteinemia
Hypobetalipoproteinemia, Familial, Apolipoprotein B - 새창 An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.
Synonyms : Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type, Apolipoprotein B Deficiency Disease, Hypobetalipoproteinemia, Familial, Apo B, Apolipoprotein B Deficiencies
Hypobetalipoproteinemias - 새창 Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption.
Synonyms : Hypo beta Lipoproteinemia, Hypobetalipoproteinemia, Hypo beta Lipoproteinemias