LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
704 codes · page 3 of 15 · every class · by category · by group · panels · answer lists · parts
Karyotype Narrative (Amniotic Fluid) 64094-6 Cells counted (Amniotic Fluid, molecular genetics method) 64095-3 Colonies counted (Amniotic Fluid, molecular genetics method) 64096-1 KIR gene allele 2DL1 or Tissue (Blood, qualitative, molecular genetics method) 64413-8 KIR gene allele 2DL2 or Tissue (Blood, qualitative, molecular genetics method) 64414-6 KIR gene allele 2DL3 or Tissue (Blood, qualitative, molecular genetics method) 64415-3 KIR gene allele 2DL4 or Tissue (Blood, qualitative, molecular genetics method) 64416-1 KIR gene allele 2DL5 or Tissue (Blood, qualitative, molecular genetics method) 64419-5 KIR gene allele 2DS1 or Tissue (Blood, qualitative, molecular genetics method) 64420-3 KIR gene allele 2DS2 or Tissue (Blood, qualitative, molecular genetics method) 64421-1 KIR gene allele 2DS3 or Tissue (Blood, qualitative, molecular genetics method) 64422-9 KIR2DS4 gene full variant or Tissue (Blood, qualitative, molecular genetics method) 64423-7 KIR2DS4 gene deletion variant or Tissue (Blood, qualitative, molecular genetics method) 64424-5 KIR gene allele 2DS5 or Tissue (Blood, qualitative, molecular genetics method) 64425-2 KIR gene allele 3DL1 or Tissue (Blood, qualitative, molecular genetics method) 64426-0 KIR gene allele 3DL2 or Tissue (Blood, qualitative, molecular genetics method) 64427-8 KIR gene allele 3DL3 or Tissue (Blood, qualitative, molecular genetics method) 64428-6 KIR gene allele 3DS1 or Tissue (Blood, qualitative, molecular genetics method) 64429-4 KIR gene allele 2DP1 or Tissue (Blood, qualitative, molecular genetics method) 64430-2 KIR3DP1 gene full variant or Tissue (Blood, qualitative, molecular genetics method) 64431-0 KIR3DP1 gene deletion variant or Tissue (Blood, qualitative, molecular genetics method) 64432-8 SEPT9 gene methylation (qualitative, molecular genetics method) 65810-4 PCA3 score (Urine, molecular genetics method) 69361-4 PCA3 score Qualitative (Urine, qualitative, molecular genetics method) 69362-2 Clinical cytogeneticist review of results 69965-2 Number of chromosome 13 present (Amniotic Fluid, naa with probe detection) 70109-4 Number of chromosome 18 present (Amniotic Fluid, naa with probe detection) 70110-2 Number of chromosome 21 present (Amniotic Fluid, naa with probe detection) 70111-0 DNA double strand in Specimen 72496-3 dic(9;20)(p11-13;q11)(wcp9+,wcp20+) or Tissue (Blood, fish nominal) 72827-9 Fetal Chromosome X and Y aneuploidy risk based on Plasma cell-free DNA (dosage of chromosome-specific cfdna) 73821-1 Chromosome X and Y aneuploidy cell-free DNA (dosage of chromosome-specific cfdna nominal) 73822-9 Cancer related multigene analysis or Tissue (Blood, molecular genetics method) 73977-1 BCR-ABL1 p210 Major Molecular Response (MMR) or Tissue (Blood, qualitative, molecular genetics method --post treatment) 74041-5 ERBB2 gene copy number/nucleus (Tissue, fish) 74860-8 Chromosome 17 copy number/nucleus (Tissue, fish) 74861-6 t(15;17)(q24.1;q21.1)(PML,RARA) fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75011-7 t(4;11)(q21.3;q23)(AFF1,MLL) fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75012-5 t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75013-3 t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75014-1 t(9;22)(q34.1;q11)(ABL1,BCR) b2a2 fusion transcript or Tissue (Blood, qualitative, molecular genetics method) 75015-8 t(9;22)(q34.1;q11)(ABL1,BCR) b3a2 fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75016-6 t(9;22)(q34.1;q11)(ABL1,BCR) e19a2 fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75017-4 t(9;22)(q34.1;q11)(ABL1,BCR) e19a2 fusion transcript or Tissue (Blood, qualitative, molecular genetics method) 75018-2 t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript (Bone Marrow, qualitative, molecular genetics method) 75019-0 t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript (Bone Marrow, molecular genetics method) 75020-8 Noninvasive prenatal testing overall interpretation Qualitative (qualitative) 75544-7 Noninvasive prenatal testing comment 75545-4 Fetal Monosomy X prior risk Based on maternal age 75566-0 Fetal Monosomy X risk based on Plasma cell-free+WBC DNA (dosage of chromosome-specific cfdna) 75567-8