| parent | Lab | LP29693-6 |
| child | Genetics results | LP70194-3 |
| child | Mitochondria whole genome analysis | LP433528-9 |
| child | Genes | LP32747-5 |
| child | Ploidy | LP32748-3 |
| child | Multigene studies | LP427513-9 |
| 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 | MOLPATH.PHARMG | LP202929-8 |
| child | Copy number variation analysis | LP433611-3 |
| child | PANEL.MOLPATH | LP62072-1 |
| PartDisplayName | en-US | MOLPATH |
| DisplayName | en-US | Molecular pathology |
LOINC Version: 2.77
FHIR