| parent | MOLPATH | LP7822-2 |
| child | Abnormal hemoglobin gene panel | LP94307-3 |
| child | Acute & chronic leukemia fusion transcript panel | LP156442-8 |
| child | Acute & chronic leukemia fusion transcript per control transcript panel | LP156443-6 |
| child | Alpha globin gene deletion panel | LP433648-5 |
| child | Alpha thalassemia gene panel | LP94306-5 |
| child | Breast cancer 10Y risk of distant recurrence panel | LP188517-9 |
| child | Chromosome analysis basic associated observations panel | LP190674-4 |
| child | Clinical genetic report summary panel | LP65485-2 |
| child | Complex variant panel | LP212294-5 |
| child | DNA analysis discrete sequence variation basic associated observations panel | LP190673-6 |
| child | F2 gene.c.20210G>A & F5 gene.c.1691G>A panel | LP417219-5 |
| child | Genechip kit panel | LP62074-7 |
| child | Haplotype definition panel | LP232214-9 |
| child | ERBB2 gene duplication associated observations panel | LP183636-2 |
| child | PANEL.HL7.CYTOGEN | LP111373-9 |
| child | HTT gene mutation panel | LP71244-5 |
| child | KIR genotyping panel | LP116662-0 |
| child | Master HL7 genetic variant reporting panel | LP212290-3 |
| child | Medication usage implications panel | LP213618-4 |
| child | Monotypic plasma cell identification & risk stratification panel | LP410828-0 |
| child | Noninvasive prenatal fetal 13 & 18 & 21 aneuploidy panel | LP189736-4 |
| child | Noninvasive prenatal fetal 18 & 21 aneuploidy panel | LP189735-6 |
| child | Noninvasive prenatal fetal aneuploidy & 22q11.2 deletion panel | LP422145-5 |
| child | Noninvasive prenatal fetal aneuploidy and microdeletion panel | LP185919-0 |
| child | Noninvasive prenatal fetal aneuploidy panel | LP173436-9 |
| child | Pharmacogenomic analysis basic associated observations panel | LP199197-7 |
| child | Pharmacogenomics result panel | LP213619-2 |
| child | Sequence variation panel | LP62071-3 |
| child | Sequencing methodology panel | LP62075-4 |
| child | Metagenomic DNA and RNA Sequencing | LP437401-5 |
| child | Simple variant panel | LP212293-7 |
| child | Spinal muscular atrophy newborn screening panel | LP288643-2 |
| child | Structural variant panel | LP212396-8 |
| child | t(9;22)(q34.1;q11)(ABL1,BCR) transcript detection panel | LP68320-8 |
| PartDisplayName | en-US | PANEL.MOLPATH |
| DisplayName | en-US | Molecular Pathology Panels |
LOINC Version: 2.77
FHIR