#ExistRefRangeSet>
Reference Interval:
#ExistRefRange>By report
*ExistRefRange>
|
*ExistRefRangeSet>
#ExistInterpDataSet>
| Interpretive Data: |
#ExistInterpData>Refer to report
Counseling and informed consent are recommended for genetic testing. Consent forms are available online at www.aruplab.com.
See Compliance Statement C: www.aruplab.com/CS
*ExistInterpData>
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*ExistInterpDataSet>
#ExistCPT>
| CPT Code(s): |
81479
|
*ExistCPT>
#ExistCrossReferences>
Cross References: |
0051348 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Deletion/Duplication
, 0051382 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Sequencing and Deletion Duplication, 0051510 Juvenile Polyposis (SMAD4) Sequencing, 0051575 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Sequencing, 0051789 Juvenile Polyposis (SMAD4) Sequencing and Deletion/Duplication, 2001976 Juvenile Polyposis (SMAD4) Deletion/Duplication, 2002470 PTEN-Related Disorders (PTEN) Sequencing and Deletion/Duplication, 2002722 PTEN-Related Disorders (PTEN) Sequencing, 2002726 PTEN-Related Disorders (PTEN) Deletion/Duplication, 2002730 RASA1-Related Disorders (RASA1) Sequencing, 2003156 Cerebral Cavernous Malformation (CCM2) Sequencing, 2003160 Cerebral Cavernous Malformation (CCM3) Sequencing, 2003164 Cerebral Cavernous Malformation (CCM1) Sequencing with Reflex to (CCM1, CCM2 and CCM3) Delet, 2003172 Cerebral Cavernous Malformation (CCM1, CCM2, and CCM3) Deletion/Duplication |
*ExistCrossReferences>