Find and Order Laboratory Tests
Dentinogenesis Imperfecta:
5,865 THB
Detects mutations in genes associated with dentinogenesis imperfecta, a genetic disorder affecting tooth development.
EDTA whole blood 6-10 ml
Genetic Panel
10368
DI Genetic Test Discolored Teeth Family History Genetic Disorders
Organophosphorous screening:
4,500 THB
Detects organophosphate compounds, used to diagnose poisoning from pesticides.
Gastric contents 20-30 ml Urine 10-20 ml Lithium Heparinized blood 3 – 5 ml
Toxicology Panel
10384
Nausea Occupational Exposure Organophosphate Poisoning Test Toxicology Vomiting
Hb Constant Spring:
3,750 THB
Detects mutations associated with Hemoglobin Constant Spring, a variant of alpha-thalassemia.
EDTA Whole blood 5 ml
Hematology Panel
10369
Anemia Family History Fatigue Genetic Disorders Hemoglobin Constant Spring Test
Hemophilia A _INT22 Invertion:
5,865 THB
Detects the INT22 inversion mutation in Hemophilia A patients.
EDTA whole blood 10 ml (minimum 6 ml)
Hemophilia Panel
10385
Bleeding Coagulation Disorders Easy Bruising Family History INT22 Inversion Test
Factor X Assay:
7,350 THB
10370
Fibroblast Growth Factor 23:
13,300 THB
Detects mutations in the FGF23 gene, associated with phosphate regulation disorders.
EDTA blood 6-10 ml
Genetic Panel
10371
Bone Pain FGF23 Gene Sequencing Genetic Disorders None Weakness
G6PD Quantitative:
4,250 THB
10372
Factor II Assay:
7,350 THB
Measures Factor II (prothrombin) activity, used to diagnose blood clotting disorders.
Na Citrate plasma 1 ml
Hematology Panel
10373
Coagulation Disorders Easy Bruising Family History Nosebleeds Prothrombin Activity Test
Glucose phosphate isomerase:
5,500 THB
Measures glucose phosphate isomerase enzyme activity, used to diagnose GPI deficiency.
EDTA whole blood 3 ml
Hemolytic Anemia Panel
10374
Anemia Fatigue Genetic Disorders GPI Deficiency Test None
HbH disease detection:
3,750 THB
Detects the HbH (Hemoglobin H) disease-causing gene, an alpha-thalassemia variant.
EDTA whole blood 5 ml
Hematology Panel
10375
Anemia Family History Fatigue Genetic Disorders Hemoglobin H Disease Detection
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