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Genomic Sequencing Procedures and Other Molecular Multianalyte Assays

Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome)

81410-81411
Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia)

81413-81414
Exome (eg, unexplained constitutional or heritable disorder or syndrome)

81415-81417
Genome (eg, unexplained constitutional or heritable disorder or syndrome)

81425-81427
Hearing loss (eg, nonsyndromic hearing loss, Usher syndrome, Pendred syndrome)

81430-81431
Solid organ neoplasm, genomic sequence analysis panel, 5-50 genes, interrogation for sequence variants and copy number variants or rearrangements, if performed

81445-81449
Targeted genomic sequence analysis panel, hematolymphoid neoplasm or disorder, 5-50 genes

81450-81451
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

81455-81456
Solid organ neoplasm, genomic sequence analysis panel

81457-81464
X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID)

81470-81471

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