LOINC Molecular pathology, mutations codes
Molecular pathology, mutations (MOLPATH.MUT): one class of the LOINC code system.
1,293 codes · page 12 of 26 · every class · by category · by group · panels · answer lists · parts
PINK1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 47968-3 PTEN gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 47969-1 SGCB gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 47970-9 SGSH gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 47971-7 TGFBR1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 47972-5 TGFBR2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 47973-3 THRB gene mutations found or Tissue (Blood, molecular genetics method nominal) 47974-1 AS gene mutations found or Tissue (Blood, molecular genetics method nominal) 48024-4 Gene mutations tested for or Tissue (Blood, molecular genetics method) 48025-1 ITGA2B gene mutations found or Tissue (Blood, molecular genetics method nominal) 48026-9 MT-ND4 gene c.G15257A or Tissue (Blood, qualitative, molecular genetics method) 48027-7 SERPINE1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48028-5 PKLR gene mutations found or Tissue (Blood, molecular genetics method nominal) 48029-3 RHCE gene allele Ee (Amniotic Fluid, molecular genetics method nominal) 48030-1 THRB gene p.Ala317Thr or Tissue (Blood, qualitative, molecular genetics method) 48032-7 TTR gene mutations found or Tissue (Blood, molecular genetics method nominal) 48033-5 PROS1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48161-4 MCOLN1 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 48330-5 BLM gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 48331-3 HFE gene c.845G>A or Tissue (Blood, qualitative, molecular genetics method) 48577-1 HFE gene c.187G>C or Tissue (Blood, qualitative, molecular genetics method) 48578-9 HFE gene c.187C>G or Tissue (Blood, qualitative, molecular genetics method) 48579-7 KCNQ1OT1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48580-5 BBS2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48598-7 CLCN1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48599-5 VPS13B gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48600-1 OPA1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48601-9 TGM1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48602-7 IgVH gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48670-4 JAK2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48726-4 NCF1+NCF2+CYBB gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48728-0 CYBA gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48729-8 NCF1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48732-2 NCF2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48733-0 CYBB gene mutations found or Tissue (Blood, molecular genetics method nominal) 48734-8 CYP21A2 gene mutations found (Amniotic Fluid, molecular genetics method nominal) 48781-9 PKHD1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48968-2 DCX gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48969-0 ELN gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48970-8 EYA1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48971-6 FGFR2 gene+FGFR3 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48972-4 MDCR gene mutations found or Tissue (Blood, molecular genetics method nominal) 48974-0 GPR143 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48975-7 POLG gene mutations found or Tissue (Blood, molecular genetics method nominal) 48976-5 SGCG gene mutations found or Tissue (Blood, molecular genetics method nominal) 48977-3 CDKL5 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 48978-1 TSC1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48979-9 TSC2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 48980-7 PAH gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 49014-4 PKHD1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 49215-7