Weblio日中中日辞典 のさくいん |
「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 retrieval
- False rib
- false ribs
- False scarlet fever
- false scotoma
- false scotomata
- False sel
- false set
- false shadow
- false signal
- false simon poplar bark
- false spermatorrhea
- false spikenard
- false spiritedness
- false statement
- false station
- false straight arterioles of kidney
- false suture
- false synchronization
- false target
- false tears
- false teeth
- false tendon
- false tendon cell
- False tissue tumor
- false tongue
- False trachoma
- false transmitter
- false transmitter concept
- false trichogyne
- False tuberculous tumor
- false tumor
- false twins
- false univalent
- False uterine contraction
- false vertebra
- False vertebrae
- false view
- false visual axis
- False vocal cord
- false vocal fold
- false voice
- false window
- False xanthoma
- false zero method
- false-alarm test
- false-bedding
- False-bedding
- false-negative
- false-negative message
- false-positive
- false-positive message
- 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
- FAMAS突擊步槍
- FAMAStújíbùqiāng
- 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
- familial megaloblastic anemia
- familial melanoma
- Familial methionine malabsorption
- familial microcephalia
- familial microcephaly
- familial microcytic anemia
- Familial motor neuron disease
- familial multiple endocrine neoplasia
- Familial multiple factor deficiency syndrome
- familial multiple lipomatosis
- Familial multiple lipoprotein-type hyperlipidemia
- familial multiple polyposis
- Familial multiple polyposis syndrome
- familial multiple telangiectasis
- familial myasthenia gravis
- familial mycosis fungoides
- familial myocardiopathy
- Familial myoplegia
- familial nanophthalmos
- Familial neoplastic disease
- familial nephritis
- Familial nephrogenic diabetes insipidus
- familial nephronophthisis
- Familial nephrotic syndrome
- familial neutropenia
- familial non-hemolytic jaundice
- familial non-reaginic food allergy
- Familial nonhemolytic bilirubinemia
- Familial normokalemic periodic paralysis
- familial nuchal rigidity
- Familial obesity
- familial osteoarthropathia
- familial osteoarthropathy of fingers
- Familial osteoarthropathy of the fingers
- familial osteodysplasia
- familial pancytopenia
- familial panmyelophthisis
- familial parathyroid hyperplasia
- Familial paroxysmal choreoathetosis
- familial paroxysmal polyserositis
- familial paroxysmal ventricular fibrillation
- Familial pericarditis
- familial periodic paralysis
- familial pheochromocytoma
- familial pigmental purpuric eruption
- Familial polyendocrine adenomatosis
- Familial polyneuropathic amyloidosis
- familial polyneuropathy
- familial polyposis coli
- Familial porphyria cutanea tarda
- familial prevalence
- familial primary amyloidosis
- familial primary cutaneous amyloidosis
- familial primary pulmonary hypertension
- Familial progressive cerebral sclerosis
- familial progressive diaphyseal dysplasia
- familial progressive hyperpigmentation
- familial progressive myoclonic epilepsy
- familial progressive spinal muscular atrophy
- Familial pseudohypoparathyroidism
- Familial pseudoinflammatory macular degeneration
- familial pseudopapilledema
- familial pulmonary hypertension
- familial pulmonary interstitial fibrosis
- familial pure depressive disease
- familial reactive collagenosis
- familial reactive perforating collagenosis
- Familial recurrent paralysis
- familial recurrent polyserositis
- Familial renal amyloidosis
- Familial renal glucosuria
- familial renal iminoglycinuria
- familial scleroderma
- familial selective vitamin B12 malabsorption
- familial sensitization
- familial sexual precocity
- familial short stature
- familial spastic paraplegia
- Familial spastic paraplegia syndrome
- familial spontaneous pneumothorax
- familial sudden death
- familial systemic lupus erythematosus
- familial transverse nasal groove
- familial tremor
- familial trifascicular block
- familial Turner phenotype
- Familial type 5 hyperlipoproteinemia
- familial urticaria pigmentosa
- familial vacuolization of leukocytes
- familial visceral amyloidosis
- familial visceral myopathy
- Familial visceral neuropathy
- familial visceral xanthomatosis
- familial vitamin D-resistant rickets
- familial vulvar dystrophy of lichen sclerosus type
- familial white folded mucosal dysplasia
- familial α-lipoprotein deficiency
- family
- family aggregation
- family antigen
- Family Attitudes Questionnaire
- family care center
- family care unit
- family chip
- family collateral relative
- family computer
- Family Dentistry
- family disruption
- Family disruption due to divorce
- Family disruption with separation
- Family disruption without divorce
- family doctor
- family dominant
- Family Drawing Depression Scale
- family farming
- family full-sibs
- family genetic variation
- family groupings
- family half sibs
- family health center
- family helper
- family heritability
- family history
- family history method
- family history negative
- Family history of alcohol abuse
- Family history of blindness and visual loss
- Family history of consanguinity
- Family history of deafness and hearing loss
- family history of diabetes
- Family history of diabetes mellitus
- Family history of diseases of the digestive system
- Family history of disorders of kidney and ureter
- Family history of eye and ear disorders
- family history of hirsutism
- Family history of leukemia
- Family history of malignant neoplasm of breast
- Family history of mental retardation
- Family history of stroke
- Family history of tobacco abuse
- family history positive
- family home
- family incidence
- Family investigation
- family machine
- Family maladjustment
- family mean
- family mean variance
- family medical doctor
- family medical history
- family medicine
- Family medicine specialist
- family mental health
- family nurse clinician
- family nurse practitioner
- family of action-binding proteins
- family of computer systems
- family of curves
- family of sets
- family pedigree analysis
- family performance
- family physician
- family planners
- family planning
- Family Planning Association
- Family planning center
- family planning evaluation
- family plot
- family plot error
- family practice clinic
- family rehabilitation training
- Family Secret White-Draining Powder
- Family Secret Yellow-Draining Powder
- family selection gain
- family selection method
- family selection system
- family set
- Family size
- Family stress
- family study
- family survey
- family systematic
- Family Tarsonemidae
- family therapy
- Family Tracking System
- family tree
- family trial
- Family Tyroglyphidae
- family unit
- family violence
- Family ~讓我們在一起
- Family ~ràngwǒménzàiyīqǐ
- Family 〜ひとつになること
- family-by-environment interaction
- family-education conference
- family-plan
- Family-related social factor
- famine
- famine dropsy
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