LOINC Molecular pathology, mutations codes
Molecular pathology, mutations (MOLPATH.MUT): one class of the LOINC code system.
1,293 codes · page 8 of 26 · every class · by category · by group · panels · answer lists · parts
MT-ND1 gene m.3460G>A or Tissue (Blood, qualitative, molecular genetics method) 40354-3 FGD1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40426-9 FGF23 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40427-7 NIPBL gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40428-5 NOD2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40429-3 TH gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40430-1 APTX gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40434-3 GJB1 gene allele 1 or Tissue (Blood, molecular genetics method nominal) 40461-6 GJB1 gene allele 2 or Tissue (Blood, molecular genetics method nominal) 40462-4 TNFRSF1A gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40463-2 SLC26A4 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40468-1 FBN1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 40471-5 WFS1 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40475-6 PARK2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40476-4 L1CAM gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40477-2 MAPT gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40478-0 RET gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40693-4 SOD1 gene allele 1 or Tissue (Blood, molecular genetics method nominal) 40833-6 SOD1 gene allele 2 or Tissue (Blood, molecular genetics method nominal) 40859-1 CNBP gene mutations found or Tissue (Blood, molecular genetics method nominal) 40871-6 CBS gene c.833T>C or Tissue (Blood, qualitative, molecular genetics method) 40872-4 CBS gene c.919G>A or Tissue (Blood, qualitative, molecular genetics method) 40873-2 AMPD1 gene p.Gln12Ter and p.Pro48Leu or Tissue (Blood, qualitative, molecular genetics method) 40876-5 CPT2 gene p.Pro50His+Ser113Leu or Tissue (Blood, qualitative, molecular genetics method) 40877-3 CPT2 gene p.Gln413FSer+Gly549Asp or Tissue (Blood, qualitative, molecular genetics method) 40878-1 PYGM gene p.Arg50Ter+Gly205Ser or Tissue (Blood, qualitative, molecular genetics method) 40930-0 MUTYH gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40959-9 SFTPB gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40961-5 SFTPC gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 40962-3 VWF gene mutations found or Tissue (Blood, molecular genetics method nominal) 40970-6 CPEO syndrome gene mutations found or Tissue (Blood, molecular genetics method nominal) 40994-6 Mitochondria Genes mutations found or Tissue (Blood, molecular genetics method nominal) 40995-3 WFS1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41042-3 VHL gene mutations found or Tissue (Blood, molecular genetics method nominal) 41043-1 UGT1A1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41044-9 TYR gene mutations found or Tissue (Blood, molecular genetics method nominal) 41045-6 TWIST1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41046-4 TSC gene mutations found or Tissue (Blood, molecular genetics method nominal) 41047-2 TNFRSF1A gene mutations found or Tissue (Blood, molecular genetics method nominal) 41049-8 TH gene mutations found or Tissue (Blood, molecular genetics method nominal) 41050-6 SPINK1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41051-4 SPAST gene mutations found or Tissue (Blood, molecular genetics method nominal) 41052-2 SMN1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41053-0 SMA gene mutations found or Tissue (Blood, molecular genetics method nominal) 41054-8 SLC26A4 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41055-5 SLC22A18 gene mutations found or Tissue (Blood, molecular genetics method nominal) 41056-3 SHOX gene mutations found or Tissue (Blood, molecular genetics method nominal) 41057-1 SH2D1A gene mutations found or Tissue (Blood, molecular genetics method nominal) 41058-9 SFTPC gene mutations found or Tissue (Blood, molecular genetics method nominal) 41059-7 SFTPB gene mutations found or Tissue (Blood, molecular genetics method nominal) 41060-5