LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
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KIT gene exon 17 targeted mutation analysis or Tissue (Blood, molecular genetics method) 87731-6 KIT gene exon 13 targeted mutation analysis or Tissue (Blood, molecular genetics method) 87732-4 KIT gene exon 8 targeted mutation analysis or Tissue (Blood, molecular genetics method) 87733-2 GALC gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 87738-1 BMPR1A and SMAD4 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 87756-3 Fetal Monosomy X risk based on Plasma cell-free DNA (qualitative, dosage of chromosome-specific cfdna qualitative) 88571-5 inv(2)(p21;p23)(EML4,ALK) fusion transcript (Tissue, qualitative, molecular genetics method) 88744-8 CDKN2A gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 89037-6 CHEK2 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 89038-4 MSH2 gene deletion+duplication and full mutation analysis and EPCAM gene exons 8 and 9 deletion and duplication mutation analysis or Tissue (Blood, molecular genetics method) 89039-2 HBB gene full mutation analysis or Chorionic villus sample (Amniotic Fluid, sequencing) 90925-9 MET gene amplification or Tissue (Blood, fish) 90926-7 SMN1 gene (Dbs, naa with probe detection) 92002-5 Spinal muscular atrophy newborn screening comment-discussion 92003-3 Spinal muscular atrophy newborn screen interpretation 92004-1 APOL1 inferred genotype from Donor 92636-0 MSH2 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 92675-8 MLH1 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 92676-6 Allelic frequency in Population 92821-8 Genomic coordinate system 92822-6 Source of population allelic frequency data 92824-2 Chromosome 7 copy number/nucleus or Tissue (Blood, fish) 92905-9 MET gene copy number/nucleus or Tissue (Blood, fish) 92906-7 MET gene copy number/Chromosome 7 copy number or Tissue (Blood, fish) 92907-5 F10 gene full mutation analysis or Tissue (Blood, sequencing) 92990-1 F13A1 and F13B gene full mutation analysis or Tissue (Blood, sequencing) 92991-9 FGA, FGB, and FGG gene full mutation analysis or Tissue (Blood, sequencing) 92992-7 PROCR gene full mutation analysis or Tissue (Blood, sequencing) 92993-5 PROS1 gene full mutation analysis or Tissue (Blood, sequencing) 92994-3 THBD gene full mutation analysis or Tissue (Blood, sequencing) 92995-0 Level of evidence 93044-6 Ehlers-Danlos syndrome multigene analysis or Tissue (Blood, molecular genetics method) 93200-4 Coronary heart disease multigene analysis or Tissue (Blood, molecular genetics method) 93201-2 Treatment to which interaction between genetic variants confers synergy or Tissue Nominal (Blood) 93343-2 Treatment to which genetic variant confers resistance or Tissue Nominal (Blood) 93344-0 Genetic variant effect on drug resistance or Tissue Narrative (Blood) 93345-7 Genetic variant effect on drug sensitivity or Tissue Narrative (Blood) 93346-5 Available treatment related to genetic variant and not to patient diagnosis or Tissue Nominal (Blood) 93347-3 Available treatment related to genetic variant and to patient diagnosis or Tissue Nominal (Blood) 93348-1 Treatment to which interaction between genetic variants confers resistance or Tissue Nominal (Blood) 93349-9 Cells with cytogenetic abnormality or Tissue (Blood, molecular genetics method) 93356-4 Monotypic plasma cell DNA ploidy (Bone Marrow, flow cytometry (fc)) 93359-8 Monotypic plasma cell DNA index (Bone Marrow, flow cytometry (fc)) 93360-6 Monotypic plasma cells in S phase/cells (Bone Marrow, flow cytometry (fc)) 93361-4 Genetic variant diagnostic significance or Tissue Narrative (Blood) 93364-8 Genetic variant prognostic significance or Tissue Narrative (Blood) 93365-5 Gene studied with no variant found or Tissue Nominal (Blood) 93366-3 Variant of unknown significance or Tissue Nominal (Blood) 93367-1 Summary of interaction between genetic variants or Tissue Narrative (Blood) 93368-9 (8;8)(q13;q21)(HEY1,NCOA2) fusion transcript (Tissue, qualitative, molecular genetics method) 93418-2