LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
704 codes · page 11 of 15 · every class · by category · by group · panels · answer lists · parts
RHD gene allele cell-free DNA Nominal--fetus 100670-9 SMN1 gene silent carrier analysis or Tissue (Blood, qualitative, molecular genetics method) 100694-9 Genetic disease analysis overall carrier interpretation or Tissue (Blood, molecular genetics method narrative) 100695-6 FCGR3A gene.p.Phe176Val or Tissue (Blood, qualitative, molecular genetics method) 100717-8 Platelet disorders multigene analysis or Tissue (Blood, sequencing) 100754-1 PALB2 gene targeted mutation analysis or Tissue (Blood, molecular genetics method) 100761-6 Mitochondria whole genome analysis or Tissue (Blood, molecular genetics method) 101152-7 inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript or Marrow (Blood, molecular genetics method) 101377-0 Lung cancer targeted gene fusion transcript analysis (Tissue, sequencing) 101378-8 BAP1 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 101381-2 FH gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 101382-0 MYC gene amplification (Tissue, fish) 101384-6 NF1 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 101385-3 RET gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 101386-1 HBA1 and HBA2 gene full mutation analysis or Tissue (Blood, molecular genetics method) 101387-9 GP1BB full mutation analysis or Tissue (Blood, molecular genetics method) 101388-7 GP1BA gene full mutation analysis or Tissue (Blood, molecular genetics method) 101389-5 GP9 gene full mutation analysis or Tissue (Blood, molecular genetics method) 101390-3 PAH gene full mutation analysis or Tissue (Blood, molecular genetics method) 101391-1 ADA gene full mutation analysis or Tissue (Blood, molecular genetics method) 101392-9 CLCN7 gene full mutation analysis or Tissue (Blood, molecular genetics method) 101393-7 Sex in Embryo (molecular genetics method) 101394-5 Preimplantation multigene analysis in Embryo (molecular genetics method) 101396-0 Copy number variation analysis or Tissue (Blood, sequencing) 101397-8 AGA gene 101537-9 AGA gene (calculation) 101540-3 FCGR3A gene.p.Phe158 (Blood, molecular genetics method nominal) 101545-2 FCGR3A gene.p.Val158 (Blood, molecular genetics method nominal) 101546-0 Myeloid sarcoma analysis or Tissue (Blood, fish) 101641-9 MYC and BCL2 rearrangements (Tissue, fish) 101651-8 T-Cell acute lymphoblastic leukemia or Tissue (Blood, fish) 101663-3 in Blood or Tissue (fish) 101664-1 Hereditary Wilms tumor multigene analysis or Tissue (Blood, molecular genetics method) 101671-6 B-cell lymphoma chromosome analysis (Tissue, fish) 101787-0 Noninvasive esophageal cancer DNA and esophageal cell screening in Esophagus (qualitative, sequencing) 101906-6 MET gene amplification or Tissue (Blood, molgen) 102039-5 HBA1 and HBA2 gene full mutation analysis or Chorionic villus sample (Amniotic Fluid, molecular genetics method) 102091-6 B-cell acute lymphocytic leukemia or Tissue (Blood, fish) 102099-9 B-cell acute lymphoblastic leukemia or Tissue (Blood, fish) 102100-5 Cell-free DNA.donor/Cell-free DNA.total (Blood, sequencing --post transplant) 103142-6 Genetic disease DNA and RNA analysis or Tissue (Blood, qualitative, molecular genetics method) 103143-4 Kidney transplant acute cellular rejection risk cell-free DNA (calculated by allomap) 103151-7 Single nucleotide polymorphisms.recipient derived cf.dna/Single nucleotide polymorphisms.total cf dna cell-free DNA (sequencing --post bone marrow transplant) 103154-1 Single nucleotide polymorphisms.donor derived cf.dna/Single nucleotide polymorphisms.total cf dna from Donor (Blood) 103155-8 PLA2G7 and PLAC8 gene expression level (Blood, molecular genetics method) 103556-7 Metagenomic DNA and RNA Sequencing 103566-6 HMEP-Hemiplegic migraine multigene analysis or Tissue (Blood, molecular genetics method) 103677-1 CTNNB1 gene targeted mutation analysis in Tumor (molecular genetics method) 103678-9 TP53 gene full mutation analysis or Tissue (Blood, molecular genetics method) 103680-5 Karyotype from Fetus Narrative (Tissue) 103714-2