Molecular pathology LP7822-2
LOINC Hierarchy
Select the title to see children of the section (▸) or the LOINC code. Select a code to view information about the section/code.
▸ Genetics results LP70194-3
▸ Mitochondria whole genome analysis LP433528-9
▸ Genes LP32747-5
▸ Ploidy LP32748-3
▸ Multigene studies LP427513-9
▸ Chromosome LP32750-9
▸ Genetic screen LP19405-7
▸ Microsatellite instability LP36464-3
▸ Karyotype LP28493-2
▸ Maternal cell contamination LP33231-9
▸ GenBank sequence accession number LP262418-9
▸ X linked heterotaxy LP62894-8
▸ Cancer risk assessment LP192128-9
▸ Identity testing LP76336-4
▸ Heart transplant acute cellular rejection risk LP200197-4
▸ Kidney transplant acute cellular rejection risk LP433666-7
▸ Platelet disorders multigene analysis LP433075-1
▸ Zygosity LP94227-3
▸ Prostate cancer multigene analysis LP432157-8
▸ Plasma cell proliferation analysis LP426512-2
▸ SMN1 gene silent carrier analysis LP432502-5
▸ Tripartite motif containing 46 LP437480-9
▸ Noninvasive colorectal cancer RNA and occult blood screening LP441376-3
▸ Noninvasive prenatal testing comment LP428617-7
▸ VWF and GP1BA gene mutation analysis LP441715-2
▸ Urea cycle disorders multigene analysis LP442261-6
▸ Tyrosine disorders multigene analysis LP442260-8
▸ Postmortem aortopathy multigene analysis LP441703-8
▸ Porphyria multigene analysis LP441747-5
▸ Phenylalanine disorders multigene analysis LP442259-0
▸ Peroxisomal disorder multigene analysis LP442258-2
▸ Offspring or Inheritance risk LP440976-1
▸ Noonan syndrome and related conditions multigene analysis LP441829-1
▸ Neuronal ceroid lipofuscinosis multigene analysis LP441746-7
▸ Methylmalonate aciduria-propionic aciduria multigene analysis LP441744-2
▸ Methylmalonate aciduria multigene analysis LP441742-6
▸ Marfan and related conditions multigene analysis LP441828-3
▸ Maple syrup urine disease multigene analysis LP441741-8
▸ Lysosomal storage disease multigene analysis LP442257-4
▸ Lung cancer screening LP440916-7
▸ Ketone disorders multigene analysis LP442256-6
▸ High DNA stainability LP441135-3
▸ Hereditary thrombosis disorders multigene analysis LP441714-5
▸ Hereditary platelet storage pool deficiency multigene analysis LP441713-7
▸ Hereditary platelet function defect multigene analysis LP441708-7
▸ Hereditary platelet disorders multigene analysis LP441709-5
▸ Hereditary nonpolyposis colorectal cancer multigene analysis LP441826-7
▸ Hereditary multigene analysis LP442253-3
▸ Hereditary erythrocytosis multigene analysis LP441750-9
▸ Hereditary bleeding disorders multigene analysis LP441705-3
▸ Hereditary bleeding disorders factor and von Willebrand multigene analysis LP441706-1
▸ Pharmacogenomics LP202929-8
▸ Copy number variation analysis LP433611-3
▸ Molecular Pathology Panels LP62072-1
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