WordNet

write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
(biology) the taxonomic group whose characteristics are used to define the next higher taxon
a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
all of the tokens of the same symbol; "the word `element contains five different types of character"
printed characters; "small type is hard to read"
identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
the 9th letter of the Roman alphabet (同)i
any of various disorders of lipoprotein and cholesterol metabolism that result in high levels of lipoprotein and cholesterol in the circulating blood

PrepTutorEJDIC

〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
家族の,家族特有の / 違伝的な,血統にあらわれる
『私は』私が
iodineの化学記号

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1. 高トリグリセリド血症患者に対するアプローチ approach to the patient with hypertriglyceridemia
2. リポ蛋白糸球体症 lipoprotein glomerulopathy
3. リポ蛋白の分類、代謝、およびアテローム性動脈硬化症における役割 lipoprotein classification metabolism and role in atherosclerosis
4. 家族性腺腫性ポリポーシスの臨床症状および診断 clinical manifestations and diagnosis of familial adenomatous polyposis
5. 膵外分泌癌の疫学および危険因子 epidemiology and risk factors for exocrine pancreatic cancer

Vascular risk factors, vascular disease, lipids and lipid targets in patients with familial dysbetalipoproteinemia: a European cross-sectional study.

Koopal C1, Retterstøl K2, Sjouke B3, Hovingh GK3, Ros E4, de Graaf J5, Dullaart RP6, Bertolini S7, Visseren FL8.
Atherosclerosis.Atherosclerosis.2015 May;240(1):90-7. doi: 10.1016/j.atherosclerosis.2015.02.046. Epub 2015 Feb 27.
BACKGROUND: Familial dysbetalipoproteinemia (FD), also known as type III hyperlipoproteinemia, is a genetic dyslipidemia characterized by elevated very low density lipoprotein (VLDL) and chylomicron remnant particles that confers increased risk of cardiovascular disease (CVD). The objective of this
PMID 25768710

Kei A1, Miltiadous G1, Bairaktari E1, Hadjivassiliou M1, Cariolou M1, Elisaf M1.
World journal of clinical cases.World J Clin Cases.2015 Apr 16;3(4):371-6. doi: 10.12998/wjcc.v3.i4.371.
Dysbetalipoproteinemia is a rare familial dyslipidemia characterized by approximately equally elevated serum cholesterol and triglyceride levels due to accumulated remnant lipoproteins in apolipoprotein E2/E2 homozygotes. It is associated with an increased risk for premature cardiovascular disease.
PMID 25879010

Malloy M1, Miller B2, Kane J1.
JAMA neurology.JAMA Neurol.2015 Apr;72(4):479. doi: 10.1001/jamaneurol.2014.4699.
PMID 25867729

Compound Heterozygotes for a Novel Mutation, Apo E1 Nagoya (Arg142Ser) and Apo E2 (Arg158Cys), with Severe Type III Hyperlipoproteinemia and Familial Hypercholesterolemia