LOINC Molecular pathology, mutations codes
Molecular pathology, mutations (MOLPATH.MUT): one class of the LOINC code system.
1,293 codes · page 9 of 26 · every class · by category · by group · panels · answer lists · parts
SDHD gene mutations found or Tissue (Blood, molecular genetics method nominal) 41061-3 SDHB gene mutations found or Tissue (Blood, molecular genetics method nominal) 41062-1 RPS6KA3 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41063-9 PYGM gene mutations found or Tissue (Blood, molecular genetics method nominal) 41064-7 PTPN11 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41065-4 PRX gene mutations found or Tissue (Blood, molecular genetics method nominal) 41066-2 PRF1 gene mutations found (Amniotic Fluid, molecular genetics method nominal) 41067-0 PRF1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41068-8 PPT1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41069-6 Peripheral neuropathy gene mutations found or Tissue (Blood, molecular genetics method nominal) 41070-4 PARK2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41071-2 PANK2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41072-0 NR0B1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41073-8 NPHS1 gene mutations found (Body Fluid, molecular genetics method nominal) 41074-6 NPHS1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41075-3 NPDC gene mutations found or Tissue (Blood, molecular genetics method nominal) 41076-1 NOTCH3 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41077-9 NIPBL gene mutations found or Tissue (Blood, molecular genetics method nominal) 41078-7 NEFL gene mutations found or Tissue (Blood, molecular genetics method nominal) 41079-5 Myotonic dystrophy gene mutations found or Tissue (Blood, molecular genetics method nominal) 41080-3 MUTYH gene mutations found or Tissue (Blood, molecular genetics method nominal) 41081-1 MT-TK gene mutations found or Tissue (Blood, molecular genetics method nominal) 41082-9 MTM1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41083-7 MSH2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41084-5 MPZ gene mutations found or Tissue (Blood, molecular genetics method nominal) 41085-2 MLH1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41086-0 Mitochondrial myopathy gene mutations found or Tissue (Blood, molecular genetics method nominal) 41087-8 MERRF gene mutations found or Tissue (Blood, molecular genetics method nominal) 41088-6 MEN1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41089-4 MELAS gene mutations found or Tissue (Blood, molecular genetics method nominal) 41090-2 MEFV gene mutations found or Tissue (Blood, molecular genetics method nominal) 41091-0 MAPT gene mutations found or Tissue (Blood, molecular genetics method nominal) 41092-8 LHON syndrome gene mutations found or Tissue (Blood, molecular genetics method nominal) 41093-6 LAMA2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41094-4 L1CAM gene mutations found or Tissue (Blood, molecular genetics method nominal) 41095-1 KEL gene allele (Amniotic Fluid, molecular genetics method nominal) 41096-9 HADHA gene c.1528G>C or Tissue (Blood, qualitative, molecular genetics method) 41097-7 GPC3 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41098-5 GLA gene mutations found or Tissue (Blood, molecular genetics method nominal) 41099-3 GJB6 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41100-9 GJB2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41101-7 GJB1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41102-5 Gene XXX mutations found or Tissue (Blood, molecular genetics method nominal) 41103-3 GBA gene mutations found or Tissue (Blood, molecular genetics method nominal) 41104-1 FSHD gene mutations found or Tissue (Blood, molecular genetics method nominal) 41105-8 FXN gene mutations found or Tissue (Blood, molecular genetics method nominal) 41106-6 FMR1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41107-4 FGF23 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41108-2 FGD1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41109-0 CSTB gene mutations found or Tissue (Blood, molecular genetics method nominal) 41110-8