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Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
7,455 THB
Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
7,245 THB
Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
Screens for carriers of 130 genetic diseases using NGS.
71,680 THB
Detects known family-specific variants, used for diagnosing inherited genetic disorders.
6,520 THB
Detects mutations in the FGF23 gene, associated with phosphate regulation disorders.
13,300 THB
Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 THB
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
Detects 5q chromosome deletion, used in diagnosing myelodysplastic syndromes.
10,500 THB
Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.
11,400 THB
Identifies mutations in the FXN gene, associated with Friedreich ataxia.
12,180 THB