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
having or involving or consisting of more than one part or entity or individual; "multiple birth"; "multiple ownership"; "made multiple copies of the speech"; "his multiple achievements in public life"; "her multiple personalities"; "a pineapple is a multiple fruit"
the product of a quantity by an integer; "36 is a multiple of 9"
a conjugated protein having a lipid component; the principal means for transporting lipids in the 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
多数の部分(要素)から成る,複合の,複式の / 倍数

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1. リポ蛋白糸球体症 lipoprotein glomerulopathy
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4. 心血管疾患と同等のリスクと確立した危険因子の概要 overview of the risk equivalents and established risk factors for cardiovascular disease
5. リポ蛋白aと心血管疾患 lipoprotein a and cardiovascular disease

The contribution of PCSK9 levels to the phenotypic severity of familial hypercholesterolemia is independent of LDL receptor genotype.

Drouin-Chartier JP1, Tremblay AJ1, Hogue JC2, Ooi TC3, Lamarche B1, Couture P4.
Metabolism: clinical and experimental.Metabolism.2015 Nov;64(11):1541-7. doi: 10.1016/j.metabol.2015.08.007. Epub 2015 Aug 20.
Autosomal dominant familial hypercholesterolemia (FH) is caused by genetic mutations in the LDL receptor (LDLR), its ligand apolipoprotein (apo) B, or proprotein convertase subtilisin/kexin type 9 (PCSK9). Although PCSK9 levels have been shown to correlate with LDL-cholesterol (LDL-C) levels in FH,
PMID 26371983

Familial hypercholesterolaemia with tuberous and tendinous xanthomas: case report and mutation analysis.

Kong MX1, Zhang Q2, Cao L1, Zhao C1, Ru GQ3, Bi Q1.
Clinical and experimental dermatology.Clin Exp Dermatol.2015 Oct;40(7):765-9. doi: 10.1111/ced.12644. Epub 2015 Mar 26.
Xanthomas are important clinical manifestations of disordered lipid metabolism, which are mostly found in patients with familial hypercholesterolaemia (FH), an inherited disorder that is predominantly caused by mutations in the low-density lipoprotein receptor gene (LDLR). Tuberous and tendinous xan
PMID 25807990

Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.

Rabacchi C1, Pisciotta L2, Cefalù AB3, Noto D3, Fresa R2, Tarugi P1, Averna M3, Bertolini S4, Calandra S5.
Atherosclerosis.Atherosclerosis.2015 Jul;241(1):79-86. doi: 10.1016/j.atherosclerosis.2015.04.815. Epub 2015 May 1.
BACKGROUND: Monogenic hypertriglyceridemia (HTG) may result from mutations in some genes which impair the intravascular lipolysis of triglyceride (TG)-rich lipoproteins mediated by the enzyme Lipoprotein lipase (LPL). Mutations in the LPL gene are the most frequent cause of monogenic HTG (familial c
PMID 25966443