Test ID WINS Wisconsin Newborn Screen, Blood Spot
Testing Algorithm
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
Reporting Name
Wisconsin Newborn ScreenSpecimen Type
Whole bloodSpecimen Minimum Volume
WINS: 4 blood spots
LDALD: 1 blood spot
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole blood | Ambient (preferred) | 365 days | |
Frozen | 365 days | ||
Refrigerated | 365 days |
Performing Laboratory

CPT Code Information
S3620
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
WINS | Wisconsin Newborn Screen | 54089-8 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
113124 | Wisconsin Newborn Screen | No LOINC Needed |
55323 | PHENYLKETONURIA: Phenylalanine | 29571-7 |
55324 | MAPLE SYRUP URINE DISEASE: Leucine | 38479-2 |
55325 | HOMOCYSTINURIA: Methionine | 63380-0 |
55326 | CITRULLINEMIA/ASA: Citrulline | 46733-2 |
55327 | TYROSINEMIA Type I: Succinylacetone | 46733-2 |
55328 | TYROSINEMIA Type II and III: Tyrosine | 46733-2 |
55329 | HYPOTHYROIDISM: TSH | 46762-1 |
55330 | ADRENAL HYPERPLASIA: 17-OHP | 46758-9 |
55331 | CYSTIC FIBROSIS: Trypsinogen | 46769-6 |
55332 | HEMOGLOBINOPATHIES: Hgb Pattern | 46740-7 |
55333 | FATTY ACID OXIDATION: Acylcarnitine Prof | 58088-6 |
55334 | ORGANIC ACIDEMIAS: Acylcarnitine Profile | 46733-2 |
55335 | GALACTOSEMIA: GALT Activity | 46737-3 |
55336 | BIOTINIDASE DEF: Biotinidase Activity | 46761-3 |
55337 | SCID-IMMUNODEFICIENCY: TREC | 62321-5 |
606121 | SPINAL MUSCULAR ATROPHY: SMN1 | 92004-1 |
Day(s) Performed
Monday through Friday