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85316:
Bloom Syndrome, Mutation Analysis, 2281del6/ins7

CPT Code Information Current Value

81209-BLM (Bloom syndrome, RecQ helicase-like) (eg, Bloom syndrome) gene analysis, 2281 del6ins7 variant


CPT Code Information Value Prior to 1/01/2013 7:01am

81209-BLM (Bloom syndrome, RecQ helicase-like) (eg, Bloom syndrome) gene analysis, 2281 del6ins7 variant

 

Amniotic Fluid Culture for Genetic Testing

88235-Tissue culture for amniotic fluid (if appropriate)

88240-Cryopreservation (if appropriate)

 

Fibroblast Culture for Genetic Testing

88233-Tissue culture, skin or solid tissue biopsy (if appropriate)

88240-Cryopreservation (if appropriate)

 

Maternal Cell Contamination, B

83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)

83909 x 2-Separation and identification by high-resolution technique (if appropriate)

83912-Interpretation and report (if appropriate)

 

For nonparticipating payers:

Bloom Syndrome, Mutation Analysis, 2281del6/ins7

83890-Molecular isolation or extraction

83892-Enzymatic digestion

83896-Nucleic acid probe, each

83900-Amplification, target, multiplex, first 2 nucleic acid sequences

83909-Separation and identification by high-resolution technique

83912-Interpretation and report

83914-Mutation identification by enzymatic ligation or primer extension, single segment, each segment

 

Amniotic Fluid Culture for Genetic Testing

88235-Tissue culture for amniotic fluid (if appropriate)

88240-Cryopreservation (if appropriate)

 

Fibroblast Culture for Genetic Testing

88233-Tissue culture, skin or solid tissue biopsy (if appropriate)

88240-Cryopreservation (if appropriate)

 

Maternal Cell Contamination, B

83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)

83909 x 2-Separation and identification by high-resolution technique (if appropriate)

83912-Interpretation and report (if appropriate)