| parent | Lab | LP29693-6 |
| child | Genetics results | LP70194-3 |
| child | TPSAB1 gene copy number | LP446584-7 |
| child | MicroRNA score of liver function | LP446972-4 |
| child | Mitochondria whole genome analysis | LP433528-9 |
| child | Genes | LP32747-5 |
| child | Ploidy | LP32748-3 |
| child | Multigene studies | LP427513-9 |
| child | Severe combined immunodeficiency multigene analysis | LP446796-7 |
| child | Red blood cell enzyme disorders multigene analysis | LP446798-3 |
| child | Myelodysplastic neoplasm chromosome analysis | LP444138-4 |
| child | Membranous nephropathy associated antigens analysis | LP444139-2 |
| child | Hypercholesterolemia multigene analysis | LP446799-1 |
| child | Homologous recombination deficiency status analysis | LP443568-3 |
| child | Hereditary hemolytic anemia multigene analysis | LP446797-5 |
| child | Hereditary gastrointestinal cancer multigene analysis | LP446802-3 |
| child | Dilated Cardiomyopathy and Left Ventricular Noncompaction Cardiomyopathy multigene analysis | LP446801-5 |
| child | Comprehensive cardiomyopathy multigene analysis | LP446803-1 |
| child | Autoinflammatory disorders multigene analysis | LP446804-9 |
| child | Arrhythmogenic cardiomyopathy multigene analysis | LP446805-6 |
| child | Chromosome | LP32750-9 |
| child | Genetic screen | LP19405-7 |
| child | Microsatellite instability | LP36464-3 |
| child | Karyotype | LP28493-2 |
| child | Maternal cell contamination | LP33231-9 |
| child | GenBank sequence accession number | LP262418-9 |
| child | X linked heterotaxy | LP62894-8 |
| child | Cancer risk assessment | LP192128-9 |
| child | Identity testing | LP76336-4 |
| child | Heart transplant acute cellular rejection risk | LP200197-4 |
| child | Kidney transplant acute cellular rejection risk | LP433666-7 |
| child | Platelet disorders multigene analysis | LP433075-1 |
| child | Zygosity | LP94227-3 |
| child | Prostate cancer multigene analysis | LP432157-8 |
| child | Plasma cell proliferation analysis | LP426512-2 |
| child | SMN1 gene silent carrier analysis | LP432502-5 |
| child | Tripartite motif containing 46 | LP437480-9 |
| child | Noninvasive colorectal cancer RNA+occult blood screening | LP441376-3 |
| child | Noninvasive prenatal testing comment | LP428617-7 |
| child | VWF and GP1BA gene mutation analysis | LP441715-2 |
| child | Urea cycle disorders multigene analysis | LP442261-6 |
| child | Tyrosine disorders multigene analysis | LP442260-8 |
| child | Postmortem aortopathy multigene analysis | LP441703-8 |
| child | Porphyria multigene analysis | LP441747-5 |
| child | Phenylalanine disorders multigene analysis | LP442259-0 |
| child | Peroxisomal disorder multigene analysis | LP442258-2 |
| child | Offspring or Inheritance risk | LP440976-1 |
| child | Noonan syndrome and related conditions multigene analysis | LP441829-1 |
| child | Neuronal ceroid lipofuscinosis multigene analysis | LP441746-7 |
| child | Methylmalonate aciduria-propionic aciduria multigene analysis | LP441744-2 |
| child | Methylmalonate aciduria multigene analysis | LP441742-6 |
| child | Marfan and related conditions multigene analysis | LP441828-3 |
| child | Maple syrup urine disease multigene analysis | LP441741-8 |
| child | Lysosomal storage disease multigene analysis | LP442257-4 |
| child | Lung cancer screening | LP440916-7 |
| child | Ketone disorders multigene analysis | LP442256-6 |
| child | High DNA stainability | LP441135-3 |
| child | Hereditary thrombosis disorders multigene analysis | LP441714-5 |
| child | Hereditary platelet storage pool deficiency multigene analysis | LP441713-7 |
| child | Hereditary platelet function defect multigene analysis | LP441708-7 |
| child | Hereditary platelet disorders multigene analysis | LP441709-5 |
| child | Hereditary nonpolyposis colorectal cancer multigene analysis | LP441826-7 |
| child | Hereditary multigene analysis | LP442253-3 |
| child | Hereditary erythrocytosis multigene analysis | LP441750-9 |
| child | Hereditary bleeding disorders multigene analysis | LP441705-3 |
| child | Hereditary bleeding disorders factor and von Willebrand multigene analysis | LP441706-1 |
| child | MOLPATH.PHARMG | LP202929-8 |
| child | Copy number variation analysis | LP433611-3 |
| child | PANEL.MOLPATH | LP62072-1 |
| STATUS | ACTIVE |
| PartDisplayName | en-US | MOLPATH |
| DisplayName | en-US | Molecular pathology |
LOINC Version: 2.81
FHIR