GUIDE NAME |
TEST NAME |
SYNONYMS |
SQ CODE |
|
Lactate |
LA, Lactate, Lactic Acid, plasma lactate |
LACT |
|
LDH |
Lactate Dehydrogenase, LD, LDH |
LDH |
|
Lactate Dehydrogenase, Fluid |
Lactate Dehydrogenase, Fluid, LD, Fluid, LDH, Fluid |
LDHF |
|
Lactate, CSF |
CSF, Lactate, Cerebrospinal Fluid, Lactate, Lactate, CSF, Lactic Acid, CSF |
LACC |
|
Lamin AC Mutation Analysis |
LGMD - (Lamin A/C Mutation Analysis), LGMD1B - ( Lamin A/C Mutation Analysis), Limb-Girdle Muscular Dystrophy Type 1B, LMNA, Lamin A/C, Laminopathy, LMNA-Related Disorders, Dilated Cardiomyopathy 1A, LMNA-Related Emery-Dreifuss Muscular Dystrophy |
MOL37 |
|
Lamotrigine |
Lamictal |
XLAMO |
|
Lead with ZNPP |
Pb (Lead with Zinc Protoporphryn), Zinc Protoporphyrin, ZnPP |
PBZN |
|
Filter Paper Lead |
|
PBFP |
|
Lead, Only |
Pb (Lead), Lead Screen, PB only |
PBO |
|
Lead, Urine |
Lead, Urine, Pb, Urine |
XLEADU |
|
Legionella Antigen Urine |
Legionella Antigen, Urine |
XLEGI |
|
Leptospira Antibody |
Leptospira Antibody |
XLEP |
|
Leukocyte Adhesion Panel |
LAD, Leukocyte Adhesion Panel, Leukocyte Function Panel, Leukocyte Function Assay |
LAD |
|
Leukocyte Separation |
Leukocyte Separation, Lymphocytes for EM, Lymphocytes for Inclusion Bodies, Lymphocytes for Electron Microscopy |
LS |
|
LGMD Familial Mutation Analysis |
LGMD Familial Mutation Analysis, Targeted Mutation Analysis LGMD, Familial LGMD , Familial Sarcoglycan (alpha beta delta gamma), Familial Calpain, Familial Dysferlin, Familial FKRP, Familial Lamin A/C, Familial ANO5, Familial myotilin, Familial CAV3 |
MOL46 |
|
Lidocaine |
Lidocaine |
XLIDO |
|
Lipase |
Lip, Lipase |
LIPA |
|
Lipase, Fluid |
Lipase, Fluid |
LIPF |
|
Lipid Profile |
Cholesterol (Lipid Profile), HDL, High Density Lipoprotein, LDL, Lipid Profile, Low Density Lipoprotein, Triglyceride, Very Low Density Lipoprotein, VLDL |
LIPP |
|
Lithium |
Li |
LI |
|
Liver Kidney Microsomal Ab |
Kidney Microsomal Antibody, Liver Kidney Microsomal Antibody, Liver Microsomal Antibody, LKM, Microsomal Antibody, Liver and Kidney |
XLKMA |
|
LKB1 Gene Characterization |
LKB1 gene, Peutz-Jeghers Syndrome |
XLKB1G |
|
Loss of Heterozygosity (LOH), Neuroblastoma |
Loss of Heterozygosity (LOH) Neuroblastoma, LOH, NBL LOH, 1p36 LOH, 11q LOH |
MOL47 |
|
Loss of Heterozygosity, Wilms Tumor |
Wilms Tumor LOH, Nephroblastoma LOH, Wilms Tumor, Wilms LOH, 1p and 16q LOH |
MOL54 |
|
Lupus Anticoagulant Workup |
LAW, Lupus Anticoagulant Workup |
LAW |
|
LH |
LH, Luteinizing Hormone, 3rd generation LH |
LH |
|
Lyme Serology |
Borrelia burgdorferi Antibody Screen, Lyme Disease Antibody (Total) Screen |
LYDS |
|
Lyme Abs,IgG / IgM Western Blot |
Lyme Disease Antibodies, Borrelia burgdorferi, Lyme Disease |
XLYMWB |
|
Immunophenotype, Lymph Node |
Tissue Immunophenotype, Lymph Node Immunophenotype |
ILN |
|
Lymph Node Pathology |
Hodgkin's Lymphoma, Lymph Node Pathology, Lymphadenopathy, Lymphoma, Non-Hodgkin's Lymphoma |
AP19 |
|
Lysosomal Enzyme |
Lysosomal Enzyme, Lysosomal storage panel |
XLYSO |
|
Lysozyme, Serum or Body Fluid |
Lysozyme, Lysozyme, Serum or Body Fluid, Muramidase |
XLME |
|