| S-adenozilmetionina în sange (SADM)* |
165 |
160 |
4712 |
| SARS-CoV-2 antigen - test rapid in secretii respiratorii* |
90 |
86 |
5307 |
| SCCA - Carcinom cu celule scuamoase** |
70 |
67 |
1584 |
| Schistosoma mansonii Ac totali (SMAH)* |
122 |
118 |
2964 |
| Schistosoma serologie (HA si EIA) - IgG forma adult si cercarii de S.mansonii, S.haematobium (SCHISA)* |
450 |
441 |
4816 |
| Schistosoma spp. - detectie ADN parazitar - PCR* |
606 |
593 |
5295 |
| Scleroza laterala amiotrofica - panel 35 de gene - PLUS, SEQ, DEL/DUP (NE2201)* |
4600 |
4600 |
5433 |
| Scleroza laterala amiotrofica sporadica / familiala - mutatia H46R* |
1680 |
1680 |
2461 |
| Scleroza laterala amiotrofica sporadica / familiala - secventierea genei SOD1* |
3240 |
3240 |
2462 |
| Scleroza tuberoasa - panel 2 gene - TSC1, TSC2 - PLUS (ON1401)* |
3600 |
3600 |
5637 |
| Scopolamina in urina (SCOU)* |
386 |
378 |
4710 |
| Screening reproductiv - panel complex de 460 de gene - PLUS, SEQ, DEL/DUP (CS0001)* |
3900 |
3900 |
5774 |
| Screening reproductiv masculin de baza - panel complex de 114 de gene - PLUS, SEQ, DEL/DUP (CS0008)* |
3400 |
3400 |
5927 |
| Screening reproductiv masculin extins - panel complex de 433 de gene - PLUS, SEQ, DEL/DUP (CS0007)* |
3900 |
3900 |
5930 |
| Sediment urinar cantitativ (hematii, leucocite)** |
45 |
43 |
2283 |
| Sediment urinar cantitativ Addis/Hamburger** |
45 |
43 |
1414 |
| Seleniu (SE)* |
143 |
138 |
1355 |
| Seleniu in sange heparinat (SEHB)* |
121 |
117 |
4532 |
| Serina in LCR (SERIL)* |
177 |
171 |
3247 |
| Serotonina Ac IgG (SEROG)* |
138 |
133 |
1520 |
| Serotonina Ac IgM (SEROM)* |
140 |
135 |
1521 |
| Serotonina in sange (SEROE)* |
155 |
150 |
1336 |
| Serotonina in ser (SERO)* |
160 |
155 |
2533 |
| Serotonina in urina (SERU24)* |
166 |
161 |
1626 |
| Sertralina (SERT)* |
423 |
414 |
4870 |
| Sex fetal (SRY) din sange matern* |
690 |
676 |
4515 |
| SHBG (sex hormon binding globulin)** |
59 |
56 |
1078 |
| Shigella Ac IgM* |
160 |
155 |
5605 |
| Shigella Ac totali* |
111 |
107 |
5002 |
| Sifilis - Anticorpi anti-Treponema pallidum, CMIA* |
56 |
53 |
4660 |
| Sifilis - RPR (calitativ) |
22 |
21 |
1219 |
| Sifilis - RPR (semicantitativ) |
40 |
38 |
1250 |
| Sifilis - TPHA (calitativ) |
40 |
38 |
1251 |
| Sifilis - TPHA (semicantitativ) |
32 |
30 |
1252 |
| Sifilis - Treponema pallidum Ac IgG - BLOT (LUEGW)* |
177 |
171 |
1885 |
| Sifilis - Treponema pallidum Ac IgM - BLOT (LUEMW)* |
194 |
188 |
1818 |
| Sifilis - Treponema pallidum ADN-PCR (LUEPCR)* |
282 |
276 |
5202 |
| Sifilis - Treponema pallidum ADN-PCR in LCR (LUEPCL)* |
282 |
276 |
2803 |
| Sifilis - VDRL in LCR (CMTL)* |
183 |
177 |
5168 |
| Siliciu in ser (SI)* |
175 |
169 |
5888 |
| Sindrom Aicardi-Goutieres - panel 7 gene - PLUS, SEQ, DEL/DUP (ME1201)* |
3600 |
3600 |
5422 |
| Sindrom Alagille - mutatia genei JAG1 - secventiere si MLPA* |
10200 |
10200 |
2918 |
| Sindrom Alagille - mutatia genei NOTCH2 - secventiere* |
13000 |
13000 |
2919 |
| Sindrom Apert - gena FGFR2 - secventiere* |
7200 |
7200 |
3605 |
| Sindrom Ataxia Telangiectasia - Louis Bar - gena ATM - secventiere NGS* |
7500 |
7500 |
4583 |
| Sindrom CADASIL (gena NOTCH3) - MLPA* |
1400 |
1400 |
5838 |
| Sindrom Criegler-Najjar tip I/II - gena UGT1A1 (CNS)* |
4500 |
4500 |
2334 |
| Sindrom Gilbert - gena UGT1A1 (MEUL)* |
601 |
601 |
1271 |
| Sindrom Niemann-Pick tip C (gena NPC1) - secventiere* |
7500 |
7500 |
3701 |
| Sindrom QT lung (LQTS) - panel 18 gene - PLUS, SEQ, DEL/DUP (CA0301)* |
3600 |
3600 |
5423 |
| Sindrom SLOS (Smith - Lemli - Opitz)* |
3575 |
3575 |
2657 |
| Sindrom Sotos - diagnostic etapa 1 - Gena NSD1 - MLPA* |
1700 |
1700 |
4724 |
| Sindrom Sotos - diagnostic etapa 2 - Gena NSD1 - secventiere* |
8800 |
8800 |
4725 |
| Sindrom Sotos - Gena NSD1 - NGS* |
5000 |
5000 |
4723 |
| Sindrom Von Hippel-Lindau - secventiere si MLPA* |
3825 |
3825 |
2740 |
| Sindrom Wolf-Hirschhorn (culturi cromosomiale si FISH)* |
2500 |
2500 |
1837 |
| Sindromul Alport - gena COL4A3 - secventiere* |
5000 |
5000 |
4800 |
| Sindromul Alport - gena COL4A4 - secventiere* |
5000 |
5000 |
4799 |
| Sindromul Alport - gena COL4A5 - secventiere* |
5000 |
5000 |
4801 |
| Sindromul Angelman - deletii si duplicatii (15q11-13-STR) - MS-MLPA* |
1100 |
1100 |
5080 |
| Sindromul Angelman (gena UBE3A) - secventiere* |
4000 |
4000 |
4537 |
| Sindromul Bartter, tip 1 (gena SLC12A1) - secventiere* |
4500 |
4500 |
4792 |
| Sindromul Bartter, tip 3 (gena CLCNKB) - secventiere* |
4500 |
4500 |
4790 |
| Sindromul Bartter, tip 3, 4B (gena CLCNKB) - MLPA* |
2350 |
2350 |
5579 |
| Sindromul Bartter, tip 4B (gena CLCNKA) - secventiere* |
4500 |
4500 |
4788 |
| Sindromul Beckwith-Wiedemann - test genetic MLPA* |
750 |
750 |
2170 |
| Sindromul Bloch–Sulzberger (Incontinentia pigmenti) - gena IKBKG - MLPA si secventiere* |
6000 |
6000 |
5044 |
| Sindromul Brugada - panel complex de 7 gene - PLUS, SEQ, DEL/DUP (CA0901)* |
3600 |
3600 |
5439 |
| Sindromul Charcot-Marie-Tooth tip 1A (CMT1A) (gena PMP22) - secventiere* |
1800 |
1800 |
4567 |
| Sindromul Charcot-Marie-Tooth tip 1A (gena PMP22) - MLPA* |
1450 |
1450 |
4716 |
| Sindromul Charcot-Marie-Tooth tip 1B, 2I, 2J, intermediar AD (gena MPZ) - secventiere Sanger* |
1800 |
1800 |
4568 |
| Sindromul CHARGE - gena CHD-7* |
5500 |
5500 |
2154 |
| Sindromul de insuficienta medulara - panel complex de 156 de gene - PLUS, SEQ, DEL/DUP (HE0801)* |
5200 |
5200 |
5444 |
| Sindromul deficientei cerebrale a creatininei (gena GAMT) - secventiere* |
2850 |
2850 |
4769 |
| Sindromul Dravet - gena SCN1A - PLUS (S01621)* |
2950 |
2850 |
6016 |
| Sindromul Dravet - gena SCN1B - secventiere* |
3300 |
3300 |
2655 |
| Sindromul Dravet - gena SCN9A - secventiere* |
9800 |
9800 |
2656 |
| Sindromul Ehlers-Danlos - panel complex de 41 de gene - PLUS, SEQ, DEL/DUP (CA0101)* |
4600 |
4600 |
5459 |
| Sindromul Ehlers-Danlos - Tip I+II (clasic) - gena COL5A1 - MLPA* |
2000 |
2000 |
2677 |
| Sindromul Ehlers-Danlos - Tip IV (vascular) - gena COL3A1 - MLPA* |
2000 |
2000 |
2679 |
| Sindromul Ehlers-Danlos - Tip VIIa+b (artrocalazia) - cei mai comuni exoni ai genelor COL1A1 si COL1A2 - MLPA* |
4000 |
4000 |
2681 |
| Sindromul Ehlers-Danlos - Tip VIIa+b (artrocalazia) - cei mai comuni exoni ai genelor COL1A1 si COL1A2 - secventiere* |
5700 |
5700 |
2680 |
| Sindromul Fahr (Calcificare idiopatica a ganglionilor bazali (IBGC)) - secventiere NGS panel 6 gene (SLC20A2, PDGFRB, PDGFB, XPR1, MYORG, JAM2_11181 bp_ID327.00)* |
6500 |
6500 |
5487 |
| Sindromul Iov - Hiperimunoglobulina E - (genele DOCK8,SPINK5,STAT3) - NGS* |
6500 |
6500 |
4420 |
| Sindromul Joubert - panel complex de 36 de gene - PLUS, SEQ, DEL/DUP (KI1001)* |
4600 |
4600 |
5466 |
| Sindromul Lesch-Nyhan, mutatia familiala cunoscuta - gena HPRT1 - Sanger* |
900 |
900 |
5843 |
| Sindromul Liddle - panel 2 gene (SCNN1B, SCNN1G) - PLUS, SEQ, DEL/DUP (CA1401)* |
3600 |
3600 |
5456 |
| Sindromul Loeys-Dietz, genele TGFBR 1 si 2, secventiere NGS (LOEYS)* |
15500 |
15500 |
4950 |
| Sindromul Marfan si tulburari asociate - panel 36 de gene - PLUS, SEQ, DEL/DUP (CA0801)* |
4600 |
4600 |
5462 |
| Sindromul MELAS - PCR-RFLP cantitativ - detectarea mutatiei m.3243G>A din gena MT-TL1 a genomului mitocondrial* |
2100 |
2100 |
1824 |
| Sindromul Menkes - analiza MLPA a genei ATP7A* |
1200 |
1200 |
4759 |
| Sindromul Menkes - secventierea genei ATP7A* |
4800 |
4800 |
4760 |
| Sindromul MERRF - PCR-RFLP cantitativ - detectarea mutatiei m.8344A>G din gena MT-TK a genomului mitocondrial* |
1900 |
1900 |
1924 |
| Sindromul mieloproliferativ cronic - gena JAK 2 exon 12 - Hot Spot* |
650 |
650 |
5840 |
| Sindromul Muenke - mutatia c.749C>G (p.Pro250Arg) a genei FGFR3 - secventiere* |
1200 |
1200 |
4509 |
| Sindromul NARP/Leigh - PCR-RFLP cantitativ - detectarea mutatiilor m.8993T>G si m.8993T>C din gena MT-ATP6 a genomului mitocondrial* |
1700 |
1700 |
3602 |
| Sindromul nefrotic - panel complex de 96 de gene - PLUS, SEQ, DEL/DUP (KI0401)* |
4600 |
4600 |
5443 |
| Sindromul Noonan - gena PTPN11 - secventiere* |
3300 |
3300 |
4679 |
| Sindromul Noonan - gena RAF1 - secventiere* |
3300 |
3300 |
4683 |
| Sindromul Noonan - gena RIT1 - secventiere* |
760 |
760 |
4681 |
| Sindromul Noonan - gena SOS1 - secventiere* |
3300 |
3300 |
4680 |
| Sindromul Noonan - panel complex de 36 de gene - PLUS, SEQ, DEL/DUP (CA0501)* |
4600 |
4600 |
5440 |
| Sindromul Noonan - panel genele MAP2K1, PTPN11, KRAS, SOS1, RAF1, BRAF, NRAS, RIT1 - NGS* |
3700 |
3700 |
4684 |
| Sindromul Prader Willi - deletii si duplicatii (15q11-13-STR) - MS-MLPA* |
1100 |
1100 |
5076 |
| Sindromul Prader-Willy (PWA)* |
2600 |
2600 |
1673 |
| Sindromul QT scurt - panel de 5 gene (CACNA1C, CACNB2, KCNH2, KCNJ2, KCNQ1) - PLUS, SEQ, DEL/DUP (CA2101)* |
3600 |
3600 |
5458 |
| Sindromul Rett atipic (gena CDKL5/STK9) - MLPA si secventiere* |
9050 |
9050 |
3295 |
| Sindromul rinichiului polichistic - gena PKD1 - secventiere si MLPA* |
16000 |
16000 |
5062 |
| Sindromul rinichiului polichistic - gena PKD1+PKD2 - secventiere si MLPA* |
16500 |
16500 |
5064 |
| Sindromul rinichiului polichistic - gena PKD2 - secventiere si MLPA* |
16000 |
16000 |
5063 |
| Sindromul TRAPS (febra hiberniana familiala) (gena TNFRSF1) - secventiere completa* |
3000 |
3000 |
4547 |
| Sindromul Wiedemann-Steiner - mutatia c.11430-6del a genei KMT2A - secventiere Sanger* |
700 |
700 |
5660 |
| Sindromul Williams-Beuren - gena 7q11 - analiza cromozomiala din limfocite, inclusiv test FISH (WB7Q)* |
1900 |
1900 |
3383 |
| Sindromul Williams-Beuren - gena 7q11 - MLPA (WB)* |
2200 |
2200 |
1674 |
| Sindromul X fragil (gena FMR1 - FRAXA) - screening, mTP-PCR* |
1500 |
1500 |
5501 |
| Sindromul X fragil (gena FMR2 - FRAXE) - screening, TP-PCR* |
1400 |
1400 |
4545 |
| Sirolimus (SIROL)* |
192 |
186 |
2034 |
| SLOS - sindromul Smith-Lemli-Opitz - gena DHCR7 - secventiere Sanger in lichid amniotic* |
1200 |
1200 |
5105 |
| Sodiu |
16 |
15 |
63 |
| Sodiu in materii fecale (NAST)* |
140 |
135 |
5781 |
| Sodiu in sange integral (NAVB)* |
85 |
81 |
3586 |
| Sodiu urinar** |
24 |
23 |
64 |
| Somatoliberina (GHRH)* |
256 |
250 |
4530 |
| Somatostatina* |
250 |
245 |
5846 |
| Sotalol (SOTAL)* |
390 |
382 |
5825 |
| SP100 Ac IgG (SP100B)* |
132 |
128 |
5349 |
| Spermocultura** |
75 |
72 |
1352 |
| Spermograma** |
190 |
184 |
1351 |
| Spironolactona (SPIRO)* |
390 |
382 |
5938 |
| Staniu in ser (SN)* |
425 |
416 |
5613 |
| Staniu in urina (SNU)* |
439 |
430 |
2909 |
| Staphylococcus Aureus MRSA - identificare** |
56 |
53 |
3116 |
| Staphylococcus Aureus Multi-Rezistent (MRSA) ADN-PCR (MRSPCR)* |
287 |
281 |
3131 |
| SteatoScreen* |
350 |
340 |
5964 |
| Stibiu in urina* |
79 |
75 |
2219 |
| Stiren in sange (STYR)* |
450 |
441 |
2210 |
| Stiripentol (STIRI)* |
182 |
176 |
4882 |
| Streptococ betahemolitic grup A - Antigen** |
51 |
48 |
2089 |
| Streptococ de grup B - depistare in cultura secretii genitale** |
78 |
74 |
4697 |
| Strongyloides anticorpi totali (IgG/IgM) - screening test (STROGE)* |
150 |
145 |
5753 |
| Substante cu caracter reducator in materii fecale (REDSST)* |
135 |
130 |
5109 |
| Succinil acetona in urina (SUCACU)* |
475 |
465 |
5787 |
| Sulf in urina (SU)* |
479 |
469 |
5495 |
| Sulfatidaza in urina (SULFU)* |
413 |
404 |
3135 |
| Sulfit test (SUU)* |
33 |
31 |
3226 |
| Sultiam - dozare (SULTI)* |
533 |
522 |
5549 |
| Superoxid-Dismutaza (SOD)* |
190 |
184 |
2570 |
| Surditate ereditara / hipoacuzie (gena GJB2) - secventiere* |
1350 |
1350 |
5491 |
| Surditate ereditara / hipoacuzie (panel gene GJB2, GJB6, OTOF) - (NGS)* |
7400 |
7400 |
4561 |
| Surditate non-sindromica / hipoacuzie - secventiere si MLPA* |
4000 |
4000 |
4794 |
| Surditate non-sindromica (gena-GJB2) - mutatia 35delG - secventiere* |
750 |
710 |
6009 |
