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 臨床檢驗項目

 

健保有給付項目依『全民健康保險醫療費用支付標準』規定收費,未給付項目依本院自費醫療收費標準規定收費

醫令代碼醫令中文名稱醫令英文名稱自費價
000X0002小兒代謝遺傳疾病檢查Test for inborn errors of metabolism2,000
000X0006新生兒篩檢(門診)Newborn screening1,030
000X0015新生兒篩檢11項(住院)-一般個案Newborn screening(partially-paid)830
000X0016血緣鑑定Paternity test8,000
000X0034纖維芽母細胞培養Fibroblast culture3,500
000X0036資料處理及郵寄報告手續費Mail fee500
000X0052新生兒篩檢11項(住院)-無補助Newborn screening(self-paid)1,030
000X0053新生兒篩檢11項(住院)-低收入戶或原住民Newborn screening(the minority)480
000X0055芳香族L-胺基酸脫羧酵素缺乏症基因分析(Aromatic L-amino Acid Decarboxylase)AADC Deficiency11,500
000X0102羊膜細胞培養及染色體分析Amniotic Fluid Cell Culture & Chromosome Analysis6,500
000X0103超音波掃瞄,羊膜穿刺術Sonagraphy for amniocentensis3,500
000X0105絨毛膜細胞培養及染色體分析Villu cell culture & chromosome analysis6,000
000X0106超音波掃瞄及絨毛膜細胞採取Sonagraphy for C.V.S.1,200
000X0108絨毛細胞染色體分析CVS for chromosome analysis5,500
000X0109婦產科家族遺傳檢查OBS/GYN familial genetic exam.5,000
000X0111產前遺傳超音波檢查Prenatal genetic sonogram500
000X0112基因諮詢Genetic counseling250
000X0120螢光原位雜交分析(基因部羊水室)Gene Analysis for Fish3,000
000X0123基因分析 Level1Genetic Analysis Level 11,500
000X0124基因分析 Level2Genetic Analysis Level 23,000
000X0125基因分析 Level3Genetic Analysis Level 38,000
000X0126基因分析 Level4Genetic Analysis Level 415,000
000X0130羊水細胞大量培養Cell culture1,500
000X0131粒線體疾病:點突變1555Mitochondria nt1555 mutation(Deafness)560
000X0132粒線體疾病:點突變3243Mitochondria nt3243 mutation(MELAS)560
000X0133粒線體疾病:點突變8344Mitochondria nt8344 mutation(MERRF)560
000X0134粒線體疾病:點突變8993Mitochondria nt8993 mutation(Leigh)560
000X0135粒線體疾病:點突變11778Mitochondria nt11778 mutation(LHON)560
000X0136脊髓小腦性共濟失調Spinocerebellar Ataxia type Ⅰ,Ⅱ,Ⅲ2,000
000X0137齒狀紅核蒼白球萎縮症Dentato-rubro-pallido-luysian atrophy1,000
000X0138脊髓小腦性共濟失調第17型Spinocerebellar Ataxia type ⅩⅦ1,000
000X0139脊髓小腦性共濟失調第6型Spinocerebellar Ataxia type Ⅵ1,000
000X0140亨丁頓舞蹈症Huntington Disease2,000
000X0141全頻光譜核型分析Spectral Karyotyping12,000
000X0145粒線體疾病:點突變10191Mitochondria nt10191 mutation(Leigh)560
000X0146粒線體疾病:點突變13513Mitochondria nt13513 mutation(MELAS)560
000X0147甘迺迪氏症基因檢查Kennedy's Disease Genetic Test1,000
000X0148粒線體疾病點突變套組Mitochondria Disease Mutation Hot Spots Panel3,300
000X0149粒線體疾病:點突變14484Mitochondrial nt14484 mutation(LHON)560
000X0150粒線體疾病:點突變3460Mitochondrial nt3460 mutation(LHON)560
000X0151粒線體電子傳遞鏈酵素活性分析Mitochondrial electron transfer chain activity assay10,000
000X0152粒線體去氧核醣核酸大片段缺失(4977bp缺失)Mitochondrial DNA large deletion(4977bp deletion)520
000X0153嚴重複合型免疫缺乏症新生兒篩檢SCID Newborn Screening150
000X0154遺傳疾病營養諮詢 (國健局補助)Metabolic disease Nutritional consultant(BHP)250
000X0155粒線體DNA拷貝數目分析MtDNA copy number quantification test2,500
000X0156粒線體DNA nt3243 A>G定量分析MtDNA nt3243 A>G quantification test2,500
000X0157生物素症新生兒篩檢Neonatal Screening of Biotinidase Disease100
000X0159第一代非侵入性產前胎兒染色體檢測Non-invasive prenatal testing18,000
000X0160第二代非侵入性產前胎兒染色體檢測Non-invasive prenatal screening 230,000
000X0161胚胎著床前基因診斷(每個胚胎)Preimplantation Genetic Diagnosis,PGD6,000
000X0162甲型海洋性貧血基因檢測x-thalassemia3,500
000X0163威爾森氏症基因檢測Wilson's disease12,000
000X0164小胖威利症及天使症候群基因檢測Prader Willi Syndrome& Angelman Syndrome6,000
000X0165雷特氏症候群基因檢測Rett Syndrome3,100
000X0166Miller Dieker症候群LIS1突變點位分析Miller Dieker Syndrome(LIS1mutation analysis)5,480
000X0167色素失調症基因檢測Incontinentia Pigmenti/ IP,NEMO gene9,000
000X0168馬凡氏症候群基因檢測Marfan's Syndrome9,000
000X0169努南氏症基因檢測Noonan Syndrome3,060
000X0170強直性肌肉失養症基因檢測Myotonic Dystrophy4,000
000X0171軟骨發育不全症基因檢測Achondroplasia7,600
000X0172迪喬治症候群基因檢測Di-George Syndrome3,260
000X0173Miller Dieker症候群LIS1基因缺失分析Miller Dieker Syndrome(LIS1deletion analysis)2,940
000X0174威廉氏症基因檢測Williams Syndrome3,260
000X0175腎上腺腦白質失養症(ALD)篩檢Screening for Adrenoleukodystrophy240
000X0176晚發型龐貝氏症篩檢(限1歲以上使用)Screening for late-onset Pompe disease (>1 years old )800
000X0177(限男性)法布瑞氏症篩檢(限7歲以上使用)(Male) Screening for Fabry disease (>7 years old)800
000X0178尿中葡萄糖四醣檢驗Urine Glc4 test2,000
000X0179Lyso-Gb3檢驗 (法布瑞氏症追蹤和帶因者檢查)Lyso-Gb3 test (follow-up and carrier of Fabry disease)1,200
000X0180氧化膽固醇檢驗 (尼曼匹克症排除和追蹤)Oxysterol test (R/O and follow-up of Niemann-Pick disease)2,000
000X0181新生兒篩檢-典型法布瑞氏症,高雪氏症,黏多醣症Fabry, Gaucher, MPSs disease screening800
000X0182TPP1酵素檢查Tripeptidyl peptidase 1 (TPP1) enzyme assay5,000
000X0183高雪氏症篩檢(限1歲以上使用)Screening for Gaucher disease (>1 years old )800
000X0200乙型海洋性貧血基因檢測B-thalassemia3,500
000X0201家族遺傳檢查(B)Family genetic exam(B)6,000
000X0202手足血緣鑑定Siblingship test13,500
000X0203分子基因檢查Molecular genetic diagnosis2,000
000X0206基因分析 Level5Genetic Analysis Level 520,000
000X0207核酸製備DNA extration500
000X0208核酸定量分析(1)DNA Q-PCR(1)500
000X0211基因掃描分析Gene Scan60
000X0212祖孫血緣鑑定Grandparentage test13,500
000X0213特殊血液染色體檢查Special chromosome5,000
000X0214龐貝氏症篩檢Screening for Pompe Disease200
000X0215甲基丙二酸Methylmalonic Acid400
000X0216兒童神經基因檢測(小)Pediatric neurogenetic analysis(level Ι)2,000
000X0217兒童神經基因檢測(大)Pediatric neurogenetic analysis(level Ⅱ )5,500
000X0218MSI分子基因檢查Microsatellite instability DNA analysis5,000
000X0219琥珀醯丙酮Succinylacetone500
000X0220腫瘤DNA萃取(研究用)Tumor DNA Extraction(ONLY RESEARCH USE)500
000X0221甲狀腺髓質癌基因檢測(有家族史)Medullary Thyroid Cancer (MTC) Genetic Test(family history)3,500
000X0222多發性內分泌腫瘤第二型基因檢測Multiple Endocrine Neoplasia,Type2(MEN2)Genetic Test3,500
000X0223偽副甲狀腺功能低下症基因檢測Pseudohypoparathyroidism(PTH) Genetic Test7,000
000X0224單一已知基因變異位點檢測Genetic Test of single known genetic variant1,500
000X0226染色體晶片分析Array CGH analysis18,000
000X0227次世代定序疾病基因突變檢測—大範圍Next-Generation Sequencing Genetic Test - Large Range30,000
000X0228多發性內分泌腫瘤第一型基因檢測Multiple Endocrine Neoplasia,Type1(MEN1) Genetic Test7,000
000X0229次世代定序結節硬化症基因突變檢測Next Generation Sequencing for Tuberous Sclerosis Complex associated Gene Mutation Test30,000
000X0230次世代定序遺傳性乳癌/卵巢癌基因變異檢測Next Generation Sequencing for Hereditary Breast/Ovarian Cancer Associated Gene Variation Test30,000
000X0231次世代定序遺傳性大腸癌基因變異檢測Next Generation Sequencing for Hereditary Gastrointestinal Cancer Syndromes Associated Gene Variation Test30,000
000X0232次世代定序心臟疾病特定基因突變檢測Next Generation Sequencing for Selected Heart Diseases Associated Genes Mutation Test30,000
000X0233次世代定序神經退化性疾病相關基因突變檢測Next Generation Sequencing for Neurodegenerative Diseases Associated Genes Mutation Test30,000
000X0234次世代定序聽損基因突變檢測Next Generation Sequencing for Deafness Gene Mutation Test30,000
000X0235甲狀腺髓質癌基因檢測(無家族史)Medullary Thyroid Cancer (MTC) Genetic Test (no family history)6,000
000X0236次世代定序多囊性腎病變相關基因變異檢測Next Generation Sequencing for PKD Associated Genes Variation Test30,000
000X0237次世代定序黃疸相關基因變異檢測Next Generation Sequencing for Jaundice Associated Genes Variation Test30,000
000X0238全新設計已知基因變異單一位點檢測Brand New Designed Genetic Testing For An Untested Variant2,840
000X0239次世代定序粒線體DNA基因變異檢測Next Generation Sequencing for Mitochondrial DNA Variation Test25,000
000X0240全面性次世代定序與Sanger定序161個耳聾相關基因突變檢測(暫不開放)Comprehensive Next Generation Sequencing and Sanger Sequencing for Deafness Associated Genes Mutation Test(161genes)48,000
000X0241次世代定序骨骼關節疾病相關基因變異檢測Next Generation Sequencing – Bone and joint diseases associated genes variation test (OI, EDS, Marfanoid)30,000
000X0242次世代定序代謝性疾病相關基因變異檢測Next Generation Sequencing – Metabolic diseases associated genes variation test (LSD, NCL, channopathy)30,000
000X0243次世代定序神經肌肉疾病相關基因變異檢測Next Generation Sequencing – Neuromuscular diseases associated genes variation test (LGMD, CMT, FAOD)30,000
000X0244次世代定序疾病基因突變檢測—中範圍Next-Generation Sequencing Genetic Test - Middle Range15,080
000X0245次世代定序疾病基因突變檢測—小範圍Next-Generation Sequencing Genetic Test - Small Range7,060
000X0247次世代定序兒童心臟疾病相關基因變異檢測​Next Generation Sequencing - Pediatric Cardiovascular disease (Channopathy, Cardiomyoapthy, Pulmonary hypertension)30,000
000X0248次世代定序乳癌/卵巢癌血循腫瘤DNA檢驗Next Generation Sequencing of Circulating Cell - free DNA in Breast and Ovarian Cancer12,000
000X0249次世代定序腸胃道癌症血循腫瘤DNA檢驗Next Generation Sequencing of Circulating Cell - free DNA in Gastrointestinal Cancer12,000
000X0250次世代定序遺傳性癌症症候群基因檢驗NGS for Hereditary Cancer Syndromes associated Gene Variant Test30,000
000X0251次世代定序腎臟疾病相關基因變異檢測Next Generation Sequencing - Renal disease (Hypokalemia, RTA)30,000
000X0252次世代定序疾病基因突變檢測—中範圍(癲癇專用)Next-Generation Sequencing Genetic Test - Middle Range(for Epilepsy)10,000