| Name | Value |
|---|---|
| CODE | 99967 |
| COMPONENT | ATYPICAL HEMOLYTIC UREMIC SYNDROME MULTIGENE ANALYSIS |
| CHECK DIGIT | 2 |
| PROPERTY | Finding |
| DATE LAST CHANGED | 2022-02-16 00:00:00 |
| CHANGE TYPE | ADD |
| TIME ASPECT | POINT |
| SYSTEM | BLD/TISS |
| SCALE TYPE | Document |
| METHOD TYPE | MOLGEN |
| CLASS | MOLPATH |
| FULLY SPECIFIED NAME | ATYPICAL HEMOLYTIC UREMIC SYNDROME MULTIGENE ANALYSIS:FIND:PT:BLD/TISS:DOC:MOLGEN |
| SHORTNAME | AHUS MULTIGENE ANALYSIS BLD/T |
| LONG COMMON NAME | ATYPICAL HEMOLYTIC UREMIC SYNDROME MULTIGENE ANALYSIS IN BLOOD OR TISSUE BY MOLECULAR GENETICS METHOD |
| COMMENTS | Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition tha t can begin in the neonatal period to adulthood and consists of hemolytic anemi a, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testin g is performed for diagnostic, prognostic, and therapeutic assessment in patient s with aHUS.[NCBI Books: NBK1367] |
| MASTER ENTRY FOR VUID | YES |
| VUID | 5342650 |
| EFFECTIVE DATE/TIME |
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