LOINC Molecular pathology, mutations codes
Molecular pathology, mutations (MOLPATH.MUT): one class of the LOINC code system.
1,293 codes · page 15 of 26 · every class · by category · by group · panels · answer lists · parts
SPAST gene + KIAA0196 gene mutations found or Tissue (Blood, molecular genetics method nominal) 53897-5 KIAA0196 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 53898-3 TGFBR1 gene+TGFBR2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 53899-1 C10orf2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 53900-7 USH2A gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 53901-5 CFTR gene mutations found (Dbs, molecular genetics method nominal) 54083-1 FLT3 gene targeted mutation analysis (Bone Marrow, molecular genetics method) 54447-8 NPM1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 54448-6 SMN2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 54449-4 BCR-ABL1 kinase domain mutations found or Tissue (Blood, molecular genetics method nominal) 55135-8 SCN5A gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 55139-0 Familial long QTS syndrome gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 55146-5 DHCR7 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 55195-2 KIT gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 55201-8 HBA2 gene c.427T>C (Blood, qualitative, molecular genetics method) 55237-2 HBA2 gene c.429A>T (Blood, qualitative, molecular genetics method) 55238-0 HBB gene c.441_442insAC (Blood, qualitative, molecular genetics method) 55239-8 HBB gene c.251G>A (Blood, qualitative, molecular genetics method) 55240-6 HBB gene c.19G>A (Blood, qualitative, molecular genetics method) 55241-4 HBB gene c.20A>T (Blood, qualitative, molecular genetics method) 55242-2 HBB gene c.364G>C (Blood, qualitative, molecular genetics method) 55243-0 HPFH-6 gene (Blood, qualitative, molecular genetics method) 55244-8 HBB gene c.220G>A (Blood, qualitative, molecular genetics method) 55245-5 HBA2 gene c.84G>C (Blood, qualitative, molecular genetics method) 55246-3 HBA1 gene c.223G>C (Blood, qualitative, molecular genetics method) 55247-1 HBB gene c.79G>A (Blood, qualitative, molecular genetics method) 55248-9 CAV3 gene targeted mutation analysis or Tissue (Blood, qualitative, molecular genetics method) 55296-8 JAK2 gene exon 12 targeted mutation analysis or Tissue (Blood, molecular genetics method) 55300-8 JAK2 gene exon 13 targeted mutation analysis or Tissue (Blood, molecular genetics method) 55301-6 EGFR gene exon 19 deletion or Tissue (Blood, qualitative, molecular genetics method) 55764-5 EGFR gene c.2156G>C+2155G>A+2155G>T or Tissue (Blood, qualitative, molecular genetics method) 55765-2 EGFR gene c.2573T>G or Tissue (Blood, qualitative, molecular genetics method) 55766-0 EGFR gene c.2582T>A or Tissue (Blood, qualitative, molecular genetics method) 55767-8 EGFR gene c.2303G>T or Tissue (Blood, qualitative, molecular genetics method) 55768-6 EGFR gene c.2369C>T or Tissue (Blood, qualitative, molecular genetics method) 55769-4 EGFR gene exon 20 insertion or Tissue (Blood, qualitative, molecular genetics method) 55770-2 ACE gene mutations found or Tissue (Blood, molecular genetics method nominal) 56022-7 MPL gene p.Ser505Asn or Tissue (Blood, qualitative, molecular genetics method) 56141-5 MPL gene p.Trp515Leu+Trp515Lys or Tissue (Blood, qualitative, molecular genetics method) 56142-3 CHIC2 gene 4q12 deletion or Tissue (Blood, fish) 56144-9 PCSK9 gene mutations found or Tissue (Blood, molecular genetics method nominal) 56158-9 LDLR gene mutations found or Tissue (Blood, molecular genetics method nominal) 56159-7 APOB gene+LDLR gene mutations found or Tissue (Blood, molecular genetics method nominal) 56752-9 CYP21A2 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 56780-0 BCHE gene mutations found or Tissue (Blood, molecular genetics method nominal) 56883-2 CYP11B1 gene mutations found or Tissue (Blood, molecular genetics method nominal) 57308-9 PRNP gene mutations found or Tissue (Blood, molecular genetics method nominal) 57309-7 SRY gene mutations found or Tissue (Blood, molecular genetics method nominal) 57310-5 CYP11B1 gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57311-3 PRNP gene mutations tested for or Tissue (Blood, molecular genetics method nominal) 57312-1