LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
704 codes · page 14 of 15 · every class · by category · by group · panels · answer lists · parts
MYOD1 targeted gene mutation analysis (Tissue, molecular genetics method) 105595-3 NTRK1 and NTRK2 and NTRK3 targeted gene mutation analysis (Tissue, molecular genetics method) 105596-1 POLE targeted gene mutation analysis (Tissue, molecular genetics method) 105597-9 SDHA and SDHB and SDHC and SDHD targeted gene mutation analysis (Tissue, molecular genetics method) 105598-7 Lung cancer screening based on Plasma cell-free DNA (qualitative, sequencing) 105603-5 Multiple myeloma minimal residual disease analysis (Bone Marrow, qualitative, naa with non-probe detection) 105941-9 Postmortem aortopathy multigene analysis or Tissue (Blood, molecular genetics method) 106052-4 HBG1 gene mutation analysis or Tissue (Blood, molecular genetics method) 106128-2 HBG2 gene mutation analysis or Tissue (Blood, molecular genetics method) 106129-0 HBG3 gene mutation analysis or Tissue (Blood, molecular genetics method) 106130-8 t(14;19)(q32;q13) (IGH, BCL3) or Marrow Qualitative (Blood, qualitative, fish) 106519-2 Laminin 332 IgG Ab (qualitative, immunofluorescence) 106532-5 P200 pemphigoid IgG Ab (qualitative, immunofluorescence) 106533-3 Collagen type VII IgG Ab (qualitative, immunofluorescence) 106534-1 Hereditary thyroid cancer multigene analysis or Tissue (Blood, molecular genetics method) 106780-0 Hereditary renal cancer multigene analysis or Tissue (Blood, molecular genetics method) 106781-8 Hereditary pancreatic cancer multigene analysis or Tissue (Blood, molecular genetics method) 106782-6 Myelodysplastic neoplasm chromosome analysis or Marrow (Blood, fish) 106783-4 Membranous nephropathy associated antigens analysis (Tissue, lc/ms/ms) 106784-2 Chromosome analysis (Blood, microarray) 107159-6 IgK gene Tube B length in base pairs in Specimen (molecular genetics method) 107196-8 IgK gene Tube A length in base pairs in Specimen (molecular genetics method) 107197-6 IgH FR3 length in base pairs in Specimen (molecular genetics method) 107198-4 IgH FR2 length in base pairs in Specimen (molecular genetics method) 107199-2 IgH FR1 length in base pairs in Specimen (molecular genetics method) 107200-8 PDGFRA gene full mutation analysis or Tissue (Blood, qualitative, sequencing) 107256-0 Homologous recombination deficiency status analysis (Tissue, qualitative, molecular genetics method) 107286-7 TPSAB1 gene copy number or Tissue (Blood, molecular genetics method) 107445-9 Severe combined immunodeficiency multigene analysis or Tissue (Blood, molecular genetics method) 107540-7 Hereditary hemolytic anemia multigene analysis or Tissue (Blood, molecular genetics method) 107541-5 Red blood cell enzyme disorders multigene analysis or Tissue (Blood, molecular genetics method) 107542-3 Hypercholesterolemia multigene analysis or Tissue (Blood, molecular genetics method) 107543-1 Chronic eosinophilia chromosome analysis or Tissue (Blood, fish) 107544-9 Dilated Cardiomyopathy and Left Ventricular Noncompaction Cardiomyopathy multigene analysis or Tissue (Blood, molecular genetics method) 107545-6 Hereditary gastrointestinal cancer multigene analysis or Tissue (Blood, molecular genetics method) 107546-4 Comprehensive cardiomyopathy multigene analysis or Tissue (Blood, molecular genetics method) 107547-2 Autoinflammatory disorders multigene analysis or Tissue (Blood, molecular genetics method) 107548-0 Arrhythmogenic cardiomyopathy multigene analysis or Tissue (Blood, molecular genetics method) 107549-8 Clonal frequency or Tissue (Blood, molecular genetics method) 107554-8 MicroRNA score of liver function in Platelet poor plasma (qualitative, calculation) 107611-6 Blood pathogen DNA in Specimen (naa with non-probe detection nominal) 108154-6 Hereditary paraganglioma-pheochromocytoma multigene analysis or Tissue (Blood, molecular genetics method) 111525-2 Gastric cancer risk (calculation) 111736-5 SMN1 gene copy number or Tissue (Blood, molecular genetics method) 111768-8 Aspergillus sp DNA in Bronchoalveolar lavage (naa with probe detection nominal) 111820-7 Aspergillus fumigatus CYP51A gene DNA TR34 and TR46 resistance mutations in Bronchoalveolar lavage (naa with probe detection nominal) 111821-5 C16:1-OH sulfatide (Dbs) 112304-1 C16:0 sulfatide (Dbs) 112305-8 Prostate cancer risk (Tissue, artificial intelligence image analysis) 112306-6 Hereditary idiopathic pulmonary fibrosis multigene analysis or Tissue (Blood, molecular genetics method) 112327-2