LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
704 codes · page 13 of 15 · every class · by category · by group · panels · answer lists · parts
Hereditary nonpolyposis colorectal cancer multigene analysis or Tissue (Blood, molecular genetics method) 105197-8 Marfan and related conditions multigene analysis or Tissue (Blood, molecular genetics method) 105198-6 Noonan syndrome and related conditions multigene analysis or Tissue (Blood, molecular genetics method) 105199-4 Hereditary multigene analysis or Tissue (Blood, molecular genetics method) 105259-6 Cystinuria multigene analysis or Tissue (Blood, molecular genetics method) 105260-4 Glycogen storage disease multigene analysis or Tissue (Blood, molecular genetics method) 105261-2 Ketone disorders multigene analysis or Tissue (Blood, molecular genetics method) 105262-0 Lysosomal storage disease multigene analysis or Tissue (Blood, molecular genetics method) 105263-8 Peroxisomal disorder multigene analysis or Tissue (Blood, molecular genetics method) 105264-6 Phenylalanine disorders multigene analysis or Tissue (Blood, molecular genetics method) 105265-3 Tyrosine disorders multigene analysis or Tissue (Blood, molecular genetics method) 105266-1 Urea cycle disorders multigene analysis or Tissue (Blood, molecular genetics method) 105267-9 Hereditary angioedema multigene analysis (Blood, molecular genetics method) 105329-7 Hereditary bleeding disorders multigene analysis in Specimen (molecular genetics method) 105330-5 Hereditary bleeding disorders factor and von Willebrand multigene analysis in Specimen (molecular genetics method) 105331-3 MYH9 gene full mutation analysis (Blood, molecular genetics method) 105332-1 Hereditary platelet function defect multigene analysis (Blood, molecular genetics method) 105333-9 Hereditary platelet disorders multigene analysis or Tissue (Blood, molecular genetics method) 105334-7 Hereditary platelet storage pool deficiency multigene analysis (Blood, molecular genetics method) 105335-4 Hereditary thrombosis disorders multigene analysis (Blood, molecular genetics method) 105336-2 VWF and GP1BA gene mutation analysis in Specimen (molecular genetics method) 105337-0 2-Hydroxyglutarate aciduria multigene analysis or Tissue (Blood, molecular genetics method) 105341-2 3-Methylglutaconate aciduria multigene analysis or Tissue (Blood, molecular genetics method) 105342-0 Acute myeloid Leukemia multigene analysis or Tissue (Blood, molecular genetics method) 105343-8 Acute porphyria multigene analysis or Tissue (Blood, molecular genetics method) 105344-6 Cholestasis multigene analysis or Tissue (Blood, molecular genetics method) 105345-3 Glycosylation congenital disorders multigene analysis or Tissue (Blood, molecular genetics method) 105346-1 Methylmalonate aciduria multigene analysis or Tissue (Blood, molecular genetics method) 105347-9 Methylmalonate aciduria-propionic aciduria multigene analysis or Tissue (Blood, molecular genetics method) 105348-7 Neuronal ceroid lipofuscinosis multigene analysis or Tissue (Blood, molecular genetics method) 105349-5 Porphyria multigene analysis or Tissue (Blood, molecular genetics method) 105350-3 Hereditary erythrocytosis multigene analysis or Tissue (Blood, molecular genetics method) 105351-1 Congenital lactic acidosis multigene analysis or Tissue (Blood, molecular genetics method) 105352-9 Fatty acid oxidation multigene analysis or Tissue (Blood, molecular genetics method) 105353-7 Glutarate aciduria 2 multigene analysis or Tissue (Blood, molecular genetics method) 105354-5 Maple syrup urine disease multigene analysis or Tissue (Blood, molecular genetics method) 105355-2 Tripartite motif containing 46 IgG Ab (CSF, qualitative, immunofluorescence) 105524-3 Tripartite motif containing 46 IgG Ab (qualitative, immunofluorescence) 105525-0 Tripartite motif containing 46 IgG Ab (CSF, immunofluorescence) 105526-8 Tripartite motif containing 46 IgG Ab (immunofluorescence) 105527-6 DICER1 gene full mutation analysis (Tissue, molecular genetics method) 105585-4 H3C14 gene targeted mutation analysis (Tissue, molecular genetics method) 105586-2 IDH1 and IDH2 genes and TERT genes targeted mutation analysis (Tissue, molecular genetics method) 105587-0 Adult type diffuse glioma gene targeted mutation analysis (Tissue, molecular genetics method) 105588-8 Bladder and Prostate cancer multigene analysis (Tissue, molecular genetics method) 105589-6 Endometrial carcinoma multigene analysis (Tissue, molecular genetics method) 105590-4 Renal cell carcinoma fibromyomatous stroma multigene analysis (Tissue, molecular genetics method) 105591-2 Gynecological carcinoma multigene analysis (Tissue, molecular genetics method) 105592-0 Renal cell carcinoma multigene analysis (Tissue, molecular genetics method) 105593-8 Ovarian, fallopian tube and peritoneal carcinoma multigene analysis (Tissue, molecular genetics method) 105594-6