LOINC Molecular pathology codes
Molecular pathology (MOLPATH): one class of the LOINC code system.
704 codes · page 5 of 15 · every class · by category · by group · panels · answer lists · parts
Vendor FISH product name or Tissue (Blood) 78042-9 Heart transplant acute cellular rejection risk in Mononuclear cells Calculated (allomap) 79102-0 Fetal Chromosome X and Y aneuploidy risk cell-free DNA Qualitative (qualitative, sequencing) 79211-9 Fetal Microdeletions risk cell-free DNA Qualitative (qualitative, sequencing) 79212-7 PMS2 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 79419-8 MLH1+MSH2+MSH6+PMS2 gene deletion+duplication and full mutation analysis or Tissue (Blood, molecular genetics method) 79570-8 PTPN22 gene.c.1858C>T or Tissue (Blood, qualitative, molecular genetics method) 81142-2 Specimen source patient identification Narrative 81147-1 Default transcript reference sequence coding system 81248-7 Default genomic reference sequence coding system 81249-5 Discrete genetic variant 81252-9 Simple variant name Nominal 81253-7 Genomic allele start-end 81254-5 dbSNP 81255-2 COSMIC 81256-0 CIGAR 81257-8 Sample variant allelic frequency 81258-6 Associated phenotype 81259-4 Complex genetic variant 81260-2 Complex variant name Nominal 81261-0 Complex variant HGVS name 81262-8 Complex variant type 81263-6 Structural variant 81286-7 Structural variant reported start-end 81287-5 Precision of boundaries Nominal 81288-3 Structural variant 81289-1 Genomic DNA change (gHGVS) 81290-9 Variant ISCN 81291-7 Simple variant 81292-5 Description of ranges of DNA sequences examined 81293-3 Genetic form configuration controls Nominal 81294-1 Other transcript reference sequence coding system OID 81295-8 Other genomic reference sequence coding system OID 81296-6 Structural variant cytogenetic location 81298-2 Structural variant reported arrCGH 81299-0 Structural variant 81300-6 Structural variant outer start and end 81301-4 Structural variant inner start and end 81302-2 HGVS version 81303-0 Variant analysis method 81304-8 Chromosome region Yp11.3 deletion AndOr rearrangement or Tissue (Blood, fish) 81748-6 Chromosome 17p13.1 deletion and 14q32 rearrangements (Bone Marrow, fish) 81751-0 Chromosome region 11p15 methylation and deletion+duplication (Amniotic Fluid, molecular genetics method) 81850-0 Chromosome region 11p15 methylation and deletion+duplication or Tissue (Blood, molecular genetics method) 81851-8 Chromosome 15 and 16 and 22 aneuploidy or Tissue (Blood, molecular genetics method) 81853-4 Karyotype or Tissue --post mitogen stimulation (Blood) 81862-5 dbSNP version 82115-7 COSMIC structural variant 82119-9 Allelic phase 82120-7 Allelic read depth 82121-5