HCS14 – “Horizon 14 (PAN-ETHNIC STANDARD)” replaced by HSS14 – “Horizon 14 (PAN-ETHNIC STANDARD)”

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Inactivated/Replace Test

Effective Date

01/24/2023

Included in Report

WML Test Directory Update | January 2023

Replacement Test

Horizon 14 (PAN-ETHNIC STANDARD)

Inactivated Test Details

Mnemonic

HCS14

Ordering Code

3302825

CPT-4 Codes(s)

81479 (or 81200, 81220, 81243, 81251, 81255, 81257, 81260, 81329, 81361, 81400, 81401, 81405, 81408, 81161)

Replacement Test Details

Mnemonic

HSS14

Ordering Code

3302872

CPT-4 Codes(s)

81479 (or 81200, 81220, 81243, 81251, 81255, 81257, 81260, 81329, 81361, 81400, 81401, 81405, 81408, 81161)

Specimen Information

Collect

Special kit

Specimen Preparation

Special kit required for blood collection. Please call lab for kit.

Transport Temperature

Room temperature

Rejection Criteria

Specimens received refrigerated or frozen

Stability

Room temperature: 7 days
Refrigerated: Unacceptable
Frozen: Unacceptable

Methodology

Copy number analysis, Next - generation sequencing, Polymerase chain reaction, Genotyping,
Sanger sequencing
more

Reference Range

See report
more

Performing Laboratory

Natera
more

New York DOH Approval Status

Yes
more

Interface Map for HSS14

Test Name Ordering Code Result Code Component Name LOINC Code AOE Prompt Units
Horizon 14 (PAN-ETHNIC STANDARD) 3302872
3302829 Ethnicity of Patient Yes
3302864 Authorize Natera to share result with partner/physician? Yes
3302827 Is this patient pregnant? Yes
3302865 Natera to follow up with patient for sample collection? Yes
3302836 Partner's DOB (MMDDYYYY) Yes
3302835 Partner's name (LAST NAME, FIRST NAME) Yes
3302866 Partner's phone number Yes
3302867 HIPAA consent obtained and available to Natera upon request Yes
3302868 Specimen type (BLOOD/SALIVA) Yes
3302826 Tay-Sachs Enzyme Add-on Yes
3302834 What type of billing? Yes
3302873 Test medically necessary/Pt. informed,consented? Yes
3302869 Report Summary 98039-1 No
3302837 Cystic Fibrosis 38404-0 No
3302838 Duchenne/Becker Muscular Dystrophy 50626-1 No
3302839 Fragile X Syndrome 64417-6 No
3302840 Spinal Muscular Atrophy 35462-1 No
3302841 Alpha-Thalassemia No
3302842 Beta-Hemoglobinopathies No
3302843 Canavan Disease No
3302844 Familial Dysautonomia No
3302845 Gaucher Disease No
3302846 Galactosemia No
3302847 Medium Chain Acyl-CoA Dehydrogenase Deficiency No
3302848 Polycystic Kidney Disease, Autosomal Recessive No
3302849 Smith-Lemli-Opitz Syndrome No
3302851 Tay-Sachs Disease (DNA only) 49253-5 No
3302853 Panel Notes No
3302854 Report Note 86467-8 No
3302855 Footnotes 62364-5 No

The CPT codes provided are for general informational purposes only and are based on an interpretation of AMA guidance. It is the sole responsibility of the billing party to determine CPT codes. Any questions regarding coding should be directed to the paying party.

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