Filter By Categories
All Categories filter
Diseases Category
Symptoms Category
Lifestyle Category
Age Groups Category
Category by Diagnostic Methods
Category by Specimen
Whole-exome sequencing of three family members (proband and both parents) to diagnose genetic disorders.
198,497 THB
Detects mutations in genes associated with treatable neurometabolic disorders.
59,080 THB
Detects mutations in genes related to metachromatic leukodystrophy, a lysosomal storage disease.
4,750 THB
Detects genetic mutations associated with Prader-Willi and Angelman syndromes.
33,600 THB
A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.
12,075 THB
Screens for carrier status of Spinal Muscular Atrophy and Fragile-X Syndrome.
23,310 THB
Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.
8,505 THB
Measures organic acids in urine, used to diagnose inborn errors of metabolism.
10,878 THB
Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.
78,750 THB