LOINC Molecular pathology, mutations codes
Molecular pathology, mutations (MOLPATH.MUT): one class of the LOINC code system.
1,293 codes · page 16 of 26 · every class · by category · by group · panels · answer lists · parts
SRY gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57314-7 IKBKG gene mutations found or Tissue (Blood, molecular genetics method nominal) 57753-6 TNFRSF13B gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57754-4 WAS gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57755-1 IKBKG gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57757-7 TNFRSF13B gene mutations found or Tissue (Blood, molecular genetics method nominal) 57758-5 WAS gene mutations found or Tissue (Blood, molecular genetics method nominal) 57759-3 AIRE gene mutations found or Tissue (Blood, molecular genetics method nominal) 57908-6 ADNFLE gene mutations found or Tissue (Blood, molecular genetics method nominal) 57909-4 CACNA1S+SCN4A gene mutations found or Tissue (Blood, molecular genetics method nominal) 57918-5 CDKN2A+CDK4 gene mutations found or Tissue (Blood, molecular genetics method nominal) 57927-6 CFTR gene p.Asp1152His or Tissue (Blood, qualitative, molecular genetics method) 57930-0 CFTR+PRSS1+SPINK1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 57931-8 CPVT1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 57951-6 DPYD2A gene targeted mutation analysis or Tissue (Blood, qualitative, molecular genetics method) 57958-1 FECH gene mutations found or Tissue (Blood, molecular genetics method nominal) 57962-3 FLCN gene mutations found or Tissue (Blood, molecular genetics method nominal) 57963-1 IDUA gene mutations found or Tissue (Blood, molecular genetics method nominal) 57983-9 KRIT1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 57990-4 MPL gene p.Trp515 or Tissue (Blood, qualitative, molecular genetics method) 58009-2 MSH2 gene+MLH1 gene+MSH6 gene mutations found or Tissue (Blood, molecular genetics method nominal) 58010-0 PKD2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 58020-9 RYR1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 58044-9 SCN4A gene mutations found or Tissue (Blood, molecular genetics method nominal) 58045-6 BRAF gene p.Val600Glu (Tissue, qualitative, molecular genetics method) 58415-1 BRAF gene mutations found or Tissue (Blood, molecular genetics method nominal) 58483-9 F12 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 58902-8 LCT gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 58924-2 F12 gene mutations found or Tissue (Blood, molecular genetics method) 58937-4 LCT gene mutations found or Tissue (Blood, molecular genetics method) 58938-2 ITGB3 gene mutations found or Tissue (Blood, molecular genetics method nominal) 58987-9 FGB gene mutations found or Tissue (Blood, molecular genetics method nominal) 58988-7 BRCA1+BRCA2 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 59041-4 ACE gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 59044-8 ITGB3 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 59045-5 FGB gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 59046-3 F5 gene p.His1299Arg or Tissue (Blood, qualitative, molecular genetics method) 59047-1 PAX6 gene targeted mutation analysis or Tissue (Blood, qualitative, molecular genetics method) 59064-6 ALAS2 gene mutations found or Tissue (Blood, molecular genetics method nominal) 59067-9 RPS19 gene targeted mutation analysis or Tissue (Blood, qualitative, molecular genetics method) 59068-7 PIK3CA gene mutations found or Tissue (Blood, molecular genetics method nominal) 60033-8 PIK3CA gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60034-6 MGMT gene methylation (Tissue, qualitative, molecular genetics method) 60252-4 IL28B gene associated variant rs12979860 or Tissue (Blood, qualitative, molecular genetics method) 60279-7 MED12 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60486-8 NPHP1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60487-6 NPHS2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60488-4 UMOD gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60490-0 LCA gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60491-8 Hypertrophic cardiomyopathy gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 60492-6