CPT® Code Set →
section notes
Pathology and Laboratory Procedures →
section notes
Genomic Sequencing Procedures and Other Molecular Multianalyte Assays →
section notes
81410‑81411   Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome)
81412   ASHKENAZI JEWISH ASSOC DSRDRS GEN SEQ ANAL 9 GEN
81413‑81414   Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia)
81415‑81417   Exome (eg, unexplained constitutional or heritable disorder or syndrome)
81418   RX METAB GENOMIC SEQ ALYS PANEL AT LEAST 6 GENES
81419   EPILEPSY GENOMIC SEQUENCE ANALYSIS PANEL
81420   FETAL CHROMOSOMAL ANEUPLOIDY GENOMIC SEQ ANALYS
81422   FETAL CHROMOSOMAL MICRODELTJ GENOMIC SEQ ANALYS
81425‑81427   Genome (eg, unexplained constitutional or heritable disorder or syndrome)
81430‑81431   Hearing loss (eg, nonsyndromic hearing loss, Usher syndrome, Pendred syndrome)
81432   HEREDITARY BRST CA-RLATD DO GEN SEQ ALYS 5+ GEN
81434   HEREDITARY RTA DO GEN SEQ ALYS AT LEAST 15 GEN
81435   HEREDITARY COLON CA-RELATED DO GEN SEQ ALYS 5+
81437   HERED NEUROEND TUM-RELATED DO GEN SEQ ALYS 5+
81439   HEREDITARY CARDIOMYOPATHY GEN SEQ ANALYS 5 GEN
81440   NUCLEAR MITOCHONDRIAL 100 GENE GENOMIC SEQ
81441   IBMFS SEQUENCE ANALYSIS PANEL AT LEAST 30 GENES
81442   NOONAN SPECTRUM DISORDERS GEN SEQ ANALYS 12 GEN
81443   GENETIC TESTING FOR SEVERE INHERITED CONDITIONS
81445‑81449   Solid organ neoplasm, genomic sequence analysis panel, 5-50 genes, interrogation for sequence variants and copy number variants or rearrangements, if performed
81448   HEREDITARY PERIPHERAL NEUROPATHY GEN SEQ PNL
81450‑81451   Targeted genomic sequence analysis panel, hematolymphoid neoplasm or disorder, 5-50 genes
81455‑81456   Solid organ or hematolymphoid neoplasm or disorder, 51 or greater genes, genomic sequence analysis panel, interrogation for sequence variants and copy number variants or rearrangements, or isoform expression or mRNA expression levels, if performed
81457‑81464   Solid organ neoplasm, genomic sequence analysis panel
81460   WHOLE MITOCHONDRIAL GENOME
81465   WHOLE MITOCHONDRIAL GENOME ANALYSIS PANEL
81470‑81471   X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID)
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