中英英中専門用語辞典
  中国語の各種専門用語の英語訳を調べることができます。 提供 日中韓辭典研究所 URL http://www.cjk.org/cjk/indexj.htm |
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「F」から始まる用語のさくいん
- 絞込み
- F
- FA
- FB
- FC
- FD
- FE
- FF
- FG
- FH
- FI
- FJ
- FK
- FL
- FM
- FN
- FO
- FP
- FQ
- FR
- FS
- FT
- FU
- FV
- FW
- FX
- FY
- FZ
- F(50音)
- F(タイ文字)
- F(数字)
- F(記号)
- false-positive reaction
- False-positive serological test for syphilis
- false-yellowflower milkwort root or herb
- falsesour cherry branchlet
- falsesour cherry drupe
- falsesour cherry fruit
- falsesour cherry fruit-juice
- falsetto
- falsetto voice
- falsework
- falsified evidence
- falsifying
- falt cells
- falt colony
- Falta syndrome
- Falx cerebelli
- Falx cerebri
- Falx inguinalis
- Falx of cerebellum
- Falx of cerebrum
- Falx septi
- Famciclovir
- familaris osteopetrosis
- familial
- familial A-V block
- Familial absence of sella turcica
- familial accumulation
- Familial acroosteolysis syndrome
- Familial Addison disease
- familial Addisonism
- familial adrenocortical deficiency
- Familial adrenocortical hypoplasia
- familial adrenocortical insufficiency
- familial aggregations
- familial aldosterone deficiency
- familial allergy
- Familial alobar holoprosencephaly
- familial alpha-lipoprotein deficiency
- familial amaurotic idiocy
- Familial amyloid heart disease
- familial amyloid neuropathy
- familial amyloidosis
- Familial amyloidosis cutis
- familial amyotrophic lateral sclerosis
- familial and hereditory inclusion body myopathy
- familial aneurysm
- familial aplastic anemia fanconi
- Familial apolipoprotein C-II deficiency
- Familial ataxia
- familial atherosclerosis treatment study
- familial atypical mole malignant melanoma
- familial atypical multiple mole melanoma
- familial autoimmune thyroiditis
- familial autonomic dysfunction
- familial autonomic dysfunction dysautonomia
- familial benign chronic pemphigus
- familial benign hypercalcemia
- familial benign hypocalciuric hypercalcemia
- Familial benign neutropenia
- Familial benign pemphigus
- familial benign symmetric lipomatosis
- Familial blepharophimosis syndrome
- familial breast cancer
- familial broad beta disease
- familial bundle branch block
- Familial C3B inhibitor deficiency syndrome
- familial C5 dysfunction
- familial calcification of basal ganglia
- familial carbohydrate-induced hyperlipidemia
- familial carcinoma
- familial cardiac conduction disturbance
- familial cardiomegaly
- familial cardiomyopathy
- familial carotenemia
- familial cerebellar atrophy
- Familial cerebello-retinal angiomatosis
- familial chloride diarrhea
- Familial chondrocalcinosis
- familial chronic glaucomatous disease
- familial chronic idiopathic jaundice
- familial cold urticaria
- familial colloid degeneration
- familial colloid degeneration of retina
- familial colon carcinoma
- familial colonic and rectal polyposis
- familial combined hyperlipidaemia
- familial combined hyperlipidemia
- familial congenital pseudoneuritis
- familial continual skin peeling
- familial corneal dystrophy
- familial cutaneous collagenoma
- familial cutaneous papillomatosis
- familial cystinuria-lysinuria
- familial cytomegalic adrenocortical hypoplasia
- familial defect of complement system
- familial degeneration lipoid
- familial delayed cold urticaria
- familial dermatitis
- familial disease
- Familial disease with storage of sterols
- familial dominant
- familial Down syndrome
- Familial dwarfism and stiff joints
- familial dysautonomia
- familial dysfunction of C5 function
- familial dyskeratotic comedones
- familial dystonia
- familial encephalopathia
- familial endocrinopathy
- Familial enlargement of the sella turcica
- Familial eosinophilia
- Familial erythrocytosis
- familial erythrophagocytic lymphohistiocytosis
- Familial essential myoclonus
- familial essential tremor
- familial exudative vitreoretinopathy
- familial factor
- familial fat-induced hyperlipemia
- Familial fat-induced hypertriglyceridemia
- familial fatal insomnia
- Familial fibrous dysplasia of jaw
- familial focal facial dermal dysplasia
- familial form
- Familial generalized articular hypermobility
- Familial generalized lipodystrophy
- familial glucocorticoid deficiency
- familial glucocorticoid suppressible aldosteronism
- familial glucose-galactose malabsorption
- familial goiter
- familial goiter and hypothyroidism
- familial goitrous cretinism
- Familial gout nephropathy
- familial granulocytopenia benign
- familial gynecomastia
- familial HDL deficiency
- familial heart block
- Familial hematuria
- Familial hemochromatosis
- familial hemolytic jaundice
- Familial hemophagocytic histiocytosis
- familial hemophagocytic reticulosis
- Familial hemorrhagic diathesis
- familial hemorrhagic nephritis
- familial hemorrhagic telangiectasia
- familial hereditary tremor
- Familial heredity
- familial high-density lipoprotein deficiency
- familial histiocytic reticulosis
- familial hyper β-lipoproteinemia
- familial hyperalphalipoproteinemia
- familial hyperbetalipoproteinemia
- familial hypercholesterolaemia
- familial hypercholesterolaemic xanthomatosis
- familial hypercholesterolemia
- familial hypercholesterolemia syndrome
- familial hyperchylomicronemia
- Familial hyperglycerolemia
- Familial hyperkalemic periodic paralysis
- familial hyperlipidemia
- familial hyperlipoproteinemia
- familial hyperparathyroidism
- Familial hyperplastic periosteal dystrophy
- familial hyperprebetalipoproteinemia
- familial hyperproinsulinemia
- familial hypertriglyceridemia
- familial hypertrophic cardiomyopathy
- Familial hypoalphalipoproteinemia
- familial hypobetalipoproteinaemia
- familial hypobetalipoproteinemia
- familial hypocalciuric hypercalcemia
- Familial hypoceruloplasminemia
- familial hypogonadism syndrome
- Familial hypokalemia
- Familial hypokalemia-hypomagnesemia
- Familial hypokalemic periodic paralysis
- Familial hypolipoproteinemia
- Familial hypomagnesemia-hypercalciuria
- familial hypoparathyroidism
- familial hypophosphatemia
- Familial hypophosphatemic osteomalacia
- familial hypophosphatemic rickets
- familial hypoplastic anemia
- familial hypothyroidism
- Familial idiopathic hyperphosphatasemia
- familial idiopathic osteoarthropathy
- familial iminoglycinuria
- familial immunity
- Familial infantile diffuse brain sclerosis
- familial inheritance
- Familial interstitial nephritis
- familial intestinal polyposis
- Familial intrahepatic cholestasis
- familial intraosseous sweating
- familial intraosseous swellings
- Familial joint instability syndrome
- Familial joint laxity
- Familial juvenile gout
- Familial juvenile macular degeneration syndrome
- familial juvenile nephrophthisis
- familial koilonychia
- Familial lichen amyloidosis
- familial lichen amyloidosus
- familial lichen planus
- Familial lipodystrophy of limbs and trunk
- familial lipomatosis
- familial lipoprotein deficiency
- familial lipoprotein lipase deficiency
- familial localized heat urticaria
- Familial LPL deficiency
- familial lymphangiectasis
- familial male hypogonadism
- familial male infertility
- familial male sex precocity
- familial malignant melanoma
- familial medullary thyroid cancer
Weblioのさくいんはプログラムで自動的に生成されているため、一部不適切なさくいんの配置が含まれていることもあります。ご了承くださいませ。お問い合わせ。
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