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Detects expansion mutations in the HTT gene, used to diagnose Huntington’s disease.
7,770 THB
Detects mutations in the immunoglobulin heavy chain variable region (IGHV), used in diagnosing chronic lymphocytic leukemia (CLL).
34,000 THB
Boosted exome sequencing for diagnosing genetic conditions, focusing on the proband (the affected individual).
120,690 THB
Whole-exome sequencing of three family members (proband and both parents) to diagnose genetic disorders.
198,497 THB
Genetic testing for hereditary connective tissue disorders, such as Ehlers-Danlos syndrome.
46,304 THB
Detects mutations in the CFTR gene, associated with cystic fibrosis.
46,304 THB
A broad genetic health screen analyzing exome sequences for various health conditions.
49,760 THB
Detects mutations associated with inherited retinal diseases, including retinitis pigmentosa.
46,304 THB
Detects mutations in NF1 and NF2 genes associated with neurofibromatosis types 1 and 2.
34,736 THB
Detects mutations in the AR gene associated with Kennedy disease, a neurodegenerative disorder.
7,770 THB
Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.
15,390 THB