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Screens for common G6PD mutations prevalent in Asian populations, associated with G6PD deficiency.
8,400 THB
Detects mutations in the MEFV gene associated with Familial Mediterranean Fever (FMF), an inflammatory disorder.
12,075 THB
Detects mutations in the HFE gene associated with hereditary hemochromatosis, a condition causing iron overload.
12,075 THB
A customized genetic panel to analyze specific genes selected by the clinician.
67,200 THB
Measures glucose phosphate isomerase enzyme activity, used to diagnose GPI deficiency.
5,500 THB
Detects mutations associated with Hemoglobin Constant Spring, a variant of alpha-thalassemia.
3,750 THB
Detects the HbH (Hemoglobin H) disease-causing gene, an alpha-thalassemia variant.
3,750 THB
Comprehensive genetic panel for detecting mutations linked to hereditary hearing loss.
107,100 THB
Identifies mutations in the GJB1 gene associated with hereditary hearing loss.
17,338 THB
Screens for carrier status of 62 genetic disorders including thalassemia, SMA, and FMR1.
35,416 THB
Comprehensive genetic carrier screening for multiple inherited conditions, designed for preconception and early pregnancy planning.
35,416 THB
Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB