| Cerner Primary Mnemonic: | MaterniT21 Plus CORE + Microdeletions and Fetal Gender |
| PDM | 245461 |
| Informatics - Workgroup | Genetics |
| Synonyms * | MATERNITMD
NIPT
NIPS |
| Display Name * | MaterniT21 Plus CORE + Microdeletions and Sex Chromosome Aneuploidy |
| Specimen Sources (combined Order Entry and Specimen Navigator) * |
|
| Specimen Types (combined Order Entry and Specimen Navigator) * |
Blood
|
| Body Fluids (types sent through AOEs) |
|
| Specimen Navigator Specimen Types |
|
| Specimen Navigator Specimen Sources |
|
| Specimen Navigator Short Name | MATERNITMD |
| Ordering info (EPIC SmartText) | For pregnancies at increased risk of fetal abnormalities, the MaterniT21 PLUS test delivers a comprehensive NIPT for the analysis of chromosomal regions including trisomies 21, 18, and 13, fetal sex, sex chromosome aneuploidies, and an enhanced sequencing series that examines seven clinically relevant microdeletions and two additional chromosomal regions, trisomies 22 and 16. |
| IP Orderable (inpatient) | Yes |
| OP Orderable (outpatient) | Yes |
AOEs *
|
| AP AOEs | |
| Special History | No |
| Build Comments | |
| Filter * | |
| Cerner Site Restrict | AML/Quest Labs
Bio Reference Laboratory
BioReference Health LLC
Counsyl Laboratory
Illumina Laboratories
LabCorp
Mayo Medical Labs
Medtox Laboratories
Northwell Health Laboratories |
Cerner Results
| Result Desc |
Result display |
Result PDM |
| XXX (Triple X Syndrome) |
XXX (Triple X Syndrome) |
225135N |
| 1p36 deletion syndrome |
1p36 deletion syndrome |
225135W |
| Performance |
Performance |
225135AB |
| Limitations of the Test |
Limitations of the Test |
225135AD |
| Trisomy 18 (Edwards Synd) |
Trisomy 18 (Edwards Synd) |
225135G |
| Test Method |
Test Method |
225135Z |
| Approved By |
Approved By |
225135E |
| 11q23 deletion (Jacobsen) |
11q23 deletion (Jacobsen) |
225135R |
| 15q11 deletion (PW Angelman) |
15q11 deletion (PW Angelman) |
225135Q |
| Performance Characteristics |
Performance Characteristics |
225135AC |
| Trisomy 16 |
Trisomy 16 |
221533AG |
| PDF |
PDF |
221533AF |
| 8q24 deletion (Langer-Giedion) |
8q24 deletion (Langer-Giedion) |
225135S |
| 4p16 deletion(Wolf-Hirschhorn) |
4p16 deletion(Wolf-Hirschhorn) |
225135U |
| Gestation |
Gestation |
225135A |
| Positive Predictive Value |
Positive Predictive Value |
225135X |
| References |
REF |
5910709 |
| Fetal Fraction |
Fetal Fraction |
1659834P |
| Estimated Due Date (EDC): |
E Due Date |
1759834B |
| Gestational Age > or = 9w: |
Gestational Age > or = 9w: |
225135B |
| Monosomy X (Turner Syndrome) |
Monosomy X (Turner Syndrome) |
225135K |
| XXY (Klinefelter Syndrome) |
XXY (Klinefelter Syndrome) |
225135M |
| About the Test |
About the Test |
225135Y |
| Lab Director Comments |
Lab Director Comments |
225135D |
| Fetal Sex |
Fetal Sex |
225135J |
| Trisomy 13 (Patau Synd) |
Trisomy 13 (Patau Synd) |
225135H |
| 5p15 deletion (Cri-du-chat) |
5p15 deletion (Cri-du-chat) |
225135T |
| Trisomy 22 |
Trisomy 22 |
221533AH |
| Note |
Note |
225135AE |
| Trisomy 21 (Down Synd) |
Trisomy 21 (Down Synd) |
225135F |
| 22q11 deletion (DiGeorge) |
22q11 deletion (DiGeorge) |
225135P |
| Test Result |
Test Result |
225135C |
| XYY (Jacobs Syndrome) |
XYY (Jacobs Syndrome) |
225135L |
| Negative Predictive Value |
Negative Predictive Value |
221533AI |
|
| PROCEDURE ID |
189707 |
| PDM |
245461 |
| ORDER DISPLAY NAME |
MaterniT21 Plus CORE + Microdeletions and Sex Chromosome Aneuploidy |
| PROCEDURE NAME |
MATERNIT21 PLUS CORE + MICRODELETIONS AND FETAL GENDER |
| PROCEDURE MASTER NUMBER |
LAB4155 |
| SHORT PROCEDURE NAME |
MATERNIT21 PLUS CORE + MICRODELETIONS AND FETAL GENDER |
| CATEGORY CODE |
1.0 |
| CATEGORY CODE RECORD NAME |
LAB BLOOD ORDERABLES |
| SYNONYMS |
MATERNITMD
NIPT
NIPS |
| CLINICALLY ACTIVE |
Yes |
| ORDERABLE |
Yes |
| PERFORMABLE |
Yes |
| FILTER GENOMICS |
|
| REFERENCE LINK URL |
https://labs.northwell.edu/epic/test/189707 |
| ORDERING INSTRUCTIONS |
|
| DEFAULT SPECIMEN TYPE |
Blood |
| SPECIMEN TYPE PICK LIST |
Blood |
| SPECIMEN TYPE LIST |
Blood |
| OP SPECIMEN TYPE LIST |
|
| SPECIMEN SOURCE PICK LIST |
Blood, Arterial
Blood, Capillary
Blood, Central Line
Blood, Venous |
| SPECIMEN SOURCE DEFAULT - MALE |
|
| SPECIMEN SOURCE DEFAULT - FEMALE |
Blood, Venous |
| SPECIMEN SOURCE LIST |
|
| OP SPECIMEN SOURCE LIST |
|
| IP LAB TEST COMPONENTS FOR REPORT |
|
| OP LAB TEST COMPONENTS FOR REPORT |
|
| ORDER QUESTIONS |
["3045300170", "3045300171", "3045300173"] |
| ORDER QUESTIONS RECORD NAME |
NH IP HOME COLLECT DATE
NH IP HOME COLLECT DAYS
NH IP HOME COLLECT MEDICALLY NECESSARY |
| INPATIENT ORDER QUESTIONS |
[] |
| INPATIENT ORDER QUESTIONS RECORD NAME |
|
| ORDER SPECIFIC QUESTION OVERRIDE |
|
| INPATIENT QUESTION OVERRIDE |
|
| LOCATION RESTRICT LIST IP |
|
| LOCATION RESTRICT LIST IP RECORD NAME |
|
| LOCATION RESTRICT LIST INCLUDE IP |
|
| LOCATION RESTRICT LIST OP |
|
| LOCATION RESTRICT LIST OP RECORD NAME |
|
| LOCATION RESTRICT LIST INCLUDES OP |
|
| EDP AMB ORDER SPECIFIC QUESTIONS RECORD NAME |
|
| EDP IP ORDER SPECIFIC QUESTIONS RECORD NAME |
|
| EDP IP SPECIMEN SOURCE |
Blood, Venous
Blood, Central Line
Blood, Arterial
Blood, Capillary |
| EDP OP SPECIMEN SOURCE |
|
| EDP IP SPECIMEN TYPE |
Blood |
| EDP OP SPECIMEN TYPE |
|
| DERIVED EDP IP BUTTONS S |
Blood, Central Line
Blood, Capillary
Blood, Arterial
Blood, Venous |
| DERIVED EDP IP BUTTONS T |
Blood |
| DERIVED EDP OP BUTTONS S |
|
| DERIVED EDP OP BUTTONS T |
|
| IP ORDERABLE |
|
| OP ORDERABLE |
|
| STANDARD LAB COMPONENTS |
|
| STANDARD LAB COMPONENTS RECORD NAME |
|
| COMPONENT DATA REQUIREMENT |
|
EPIC OP AOEs
| Question ID | Question Name | Question | Response Type | Response List | Require Response |
|---|
| 3045300170 |
NH IP HOME COLLECT DATE |
Start Date |
Date |
|
Yes |
| 3045300171 |
NH IP HOME COLLECT DAYS |
Days |
Custom List |
Monday
Tuesday
Wednesday
Thursday
Friday
Saturday
Sunday |
Yes |
| 3045300173 |
NH IP HOME COLLECT MEDICALLY NECESSARY |
Medically Necessary? |
Yes/No |
|
Yes |
|
EPIC IP AOEs
|
EPIC Components (results - crosswalked through Cerner)
| Component ID | Component Name | Base Name | Common Name | External Name | Cerner Result PDM |
|---|
| 3047806774.0 |
XXX (TRIPLE X SYNDROME) |
XXX |
XXX TRIPLE X SYNDROME |
Xxx (Triple X Syndrome) |
225135N |
| 3047800768.0 |
1P36 DELETION SYNDROME RESULT |
1P36DELSYN |
1P36DELSYN |
|
225135W |
| 3047806804.0 |
PERFORMANCE |
PERFORMANCE |
PERFORMANCE |
Performance |
225135AB |
| 3046400004.0 |
LIMITATIONS OF THE TEST |
LIMITOFTEST |
LIMITATIONS OF THE TEST |
LIMITATIONS OF THE TEST |
225135AD |
| 3046400007.0 |
TRISOMY 18 (EDWARDS SYND) |
TRISOMY18 |
TRISOMY 18 (EDWARDS SYND) |
TRISOMY 18 (EDWARDS SYND) |
225135G |
| 3047804929.0 |
TEST METHOD |
TESTMETH |
TEST METHOD |
Test Method |
225135Z |
| 3047806828.0 |
APPROVED BY |
APPORVEDBY |
APPROVED BY |
Approved By |
225135E |
| 3047806834.0 |
11Q23 DELETION (JACOBSEN) |
11Q23DELET |
11Q23 DELETION JACOBSEN |
11Q23 Deletion (Jacobsen) |
225135R |
| 3047806293.0 |
15Q11 DELETION (PW ANGELMAN) |
15Q11DELET |
15Q11 DELETION PW ANGELMAN |
15Q11 Deletion (Pw Angelman) |
225135Q |
| 3047806803.0 |
PERFORMANCE CHARACTERISTICS |
PERFOMCHAR |
PERFORMANCE CHARACTERISTICS |
Performance Characteristics |
225135AC |
| 3048801205.0 |
TRISOMY 16 |
TRIS16 |
TRISOMY 16 |
|
221533AG |
| 3047805610.0 |
PDF AFP RESULT |
PDF |
PDF, RESULT |
Pdf Afp Result |
221533AF |
| 3047806830.0 |
8Q24 DELETION (LANGER-GIEDION) |
8Q24DELET |
8Q24 DELETION LANGER GIEDION |
8Q24 Deletion (Langer-Giedion) |
225135S |
| 3047806831.0 |
4P16 DELETION(WOLF-HIRSCHHORN) |
4P16DELET |
4P16 DELETION WOLF HIRSCHHORN |
4P16 Deletion(Wolf-Hirschhorn) |
225135U |
| 3047806196.0 |
GESTATION |
GESTATION |
GESTATION |
Gestation |
225135A |
| 3047806425.0 |
POSITIVE PREDICTIVE VALUE |
POSPREDVAL |
POSITIVE PREDICTIVE VALUE |
Positive Predictive Value |
225135X |
| 3047804491.0 |
REFERENCES |
REFERENCES |
REFERENCES |
References |
5910709 |
| 3047802440.0 |
FETAL FRACTION |
FETALFRACT |
FETAL FRACTION |
|
1659834P |
| 3047802251.0 |
E DUE DATE |
EDUEDT |
E DUE DATE |
E Due Date |
1759834B |
| 3047806197.0 |
GESTATIONAL AGE > OR = 9W: |
GESTAGE |
GESTATIONAL AGE GREATER THAN OR EQUAL TO 9W |
Gestational Age > Or = 9W: |
225135B |
| 3047805897.0 |
MONOSOMY X (TURNER SYNDROME) |
MONOSOMYX |
MONOSOMY X TURNER SYNDROME |
Monosomy X (Turner Syndrome) |
225135K |
| 3047806795.0 |
XXY (KLINEFELTER SYNDROME) |
XXY |
XXY KLINEFELTER SYNDROME |
Xxy (Klinefelter Syndrome) |
225135M |
| 3047806440.0 |
ABOUT THE TEST |
ABOUTTEST |
ABOUT THE TEST |
About The Test |
225135Y |
| 3047806408.0 |
LAB DIRECTOR COMMENTS |
LABDIRCOM |
LAB DIRECTOR COMMENTS |
Lab Director Comments |
225135D |
| 3047805983.0 |
FETAL SEX |
FETALSEX |
FETAL SEX |
Fetal Sex |
225135J |
| 3046400008.0 |
TRISOMY 13 (PATAU SYND) |
TRISOMY13 |
TRISOMY 13 (PATAU SYND) |
TRISOMY 13 (PATAU SYND) |
225135H |
| 3047806294.0 |
5P15 DELETION (CRI-DU-CHAT) |
5P15DELET |
5P15 DELETION CRI DU CHAT |
5P15 Deletion (Cri-Du-Chat) |
225135T |
| 3048801197.0 |
TRISOMY 22 |
TRIS22 |
TRISOMY 22 |
|
221533AH |
| 3046400005.0 |
NOTE |
NOTE |
NOTE |
NOTE |
225135AE |
| 3046400006.0 |
TRISOMY 21 (DOWN SYND) |
TRISOMY21 |
TRISOMY 21 (DOWN SYND) |
TRISOMY 21 (DOWN SYND) |
225135F |
| 3047806832.0 |
22Q11 DELETION (DIGEORGE) |
22Q11DELET |
22Q11 DELETION DIGEORGE |
22Q11 Deletion (Digeorge) |
225135P |
| 3047806701.0 |
TEST RESULT |
TESTRESULT |
TEST RESULT |
Test Result |
225135C |
| 3047806794.0 |
XYY (JACOBS SYNDROME) |
XYY |
XYY JACOBS SYNDROME |
Xyy (Jacobs Syndrome) |
225135L |
| 3048801196.0 |
NEGATIVE PREDICTIVE VALUE |
NEGPREDVAL |
NEGATIVE PREDICTIVE VALUE |
|
221533AI |
|
