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Factor VII Assay:

3,750 THB

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Measures Factor VII activity, used to assess bleeding disorders or clotting function.
Na Citrate plasma 2 ml
Coagulation Panel
10728
Bruising Clotting Disorders Excessive Bleeding Factor VII Activity Test None Proconvertin Test

Myriad myRisk:

234,000 THB

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A multi-gene panel test for hereditary cancer risk assessment using next-generation sequencing (NGS).
7 ml EDTA whole blood (in special collection kit) Myriad 6 ml BML SPM
Cancer Genetic Panel
10744
Family History Hereditary Cancer MyRisk Genetic Testing None Tumor Growth

Plasma for Amino Acid:

6,825 THB

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Measures plasma amino acids, used to diagnose metabolic disorders.
Heparin whole blood 3 ml (minimum volume 2 ml)
Metabolic Panel
10729
Amino Acid Plasma Test Developmental Delay Metabolic Disorders None Seizures

Urine Organic Acid:

9,188 THB

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Detects organic acids in urine, useful for diagnosing metabolic disorders.
First morning urine 30 ml (frozen if cannot perform in same day) minimum 5-10 ml
Metabolic Panel
10745
Fatigue GC-MS Urine Test Metabolic Disorders None Organic Acid Test Urinary Organic Acid Profile Weakness

Galactomannan Antigen for Aspergillus:

3,458 THB

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Detects galactomannan antigen, a marker for invasive Aspergillus infections.
Clotted blood( whole blood) 3 ml (Shipping on ice ) or Serum 2 mL Frozen
Fungal Infection Panel
10730
Aspergillus Galactomannan Test Cough Fever Fungal Infections None

Factor XII Assay:

3,750 THB

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Measures Factor XII activity, used to assess clotting function and diagnose bleeding disorders.
Na Citrate plasma 2 ml
Coagulation Panel
10731
Clotting Disorders Excessive Bleeding Factor XII Activity Test None

Factor VIII Assay:

3,750 THB

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Measures Factor VIII activity, used to diagnose hemophilia A and other clotting disorders.
Na Citrate plasma 2 ml
Coagulation Panel
10732
Bruising Clotting Disorders Excessive Bleeding Factor VIII Activity Test None

Crigler-Najjar:

11,875 THB

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Detects mutations associated with Crigler-Najjar syndrome, a rare genetic disorder affecting bilirubin metabolism.
EDTA Whole Blood 3 ml.
Genetic Disorder Panel
10733
Crigler-Najjar Genetic Test Fatigue Genetic Disorders Jaundice None

VMA:

2,160 THB

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Measures VMA levels to assess catecholamine metabolism, used for diagnosing adrenal tumors.
24 Hr Urine (preserved by 30 ml of 6N HCl ) 50 ml , minimum volume 5 ml
Adrenal Function Panel
10734
Adrenal Disorders Hypertension None Pheochromocytoma Sweating Vanillylmandelic Acid Test

IGHV somatic mutation:

34,000 THB

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Detects mutations in the immunoglobulin heavy chain variable region (IGHV), used in diagnosing chronic lymphocytic leukemia (CLL).
EDTA whole blood 3 ml. or EDTA bone marrow 3 ml.
Genetic Disorder Panel
10726
Cancer Family History Fatigue Genetic Disorders IGHV Gene Mutation Test Weakness

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