Lab Tests Directory
Browse our comprehensive catalog of medical tests. Book online and get tested at home or at any of our partner labs across all 7 Emirates.
Microarray 315k (Products of conception)
This blood test uses microarray technology to analyze genetic material, often in cases related to products of conception (tissue from miscarriage or stillbirth). It helps identify chromosomal abnormalities that may have contributed to pregnancy loss.
Microarray 750K + NGS Whole Exome Sequencing
This comprehensive blood test combines microarray analysis for detecting large chromosomal changes with Whole Exome Sequencing (WES) to identify specific gene mutations. It offers a detailed look into your genetic makeup.
Microsporidium Detection by smear examination
This test involves a microscopic examination of a stool sample to detect the presence of Microsporidium parasites. These tiny organisms can cause gastrointestinal infections.
Mitochondrial DNA Sequencing
This blood test analyzes the entire genetic material found within your mitochondria, the "powerhouses" of your cells. It looks for specific mutations that can cause mitochondrial disorders.
Mobiluncus spp. PCR
This test detects the presence of Mobiluncus species bacteria in a urine sample using PCR technology. It helps identify specific bacteria that can cause certain infections.
MRSA (Methicillin Resistant Staphylococcus aureus) DNA Detection by PCR
This test uses PCR technology to detect the DNA of Methicillin-Resistant Staphylococcus aureus (MRSA) from a swab sample. MRSA is a type of staph bacteria that is resistant to several common antibiotics.
MSI PCR
Microsatellite Instability (MSI) PCR is a test that checks for changes in specific repetitive DNA sequences called microsatellites. These changes can indicate a defect in the DNA mismatch repair system, which is important for correcting errors during DNA replication.
MTHFR (C677T and 1298C) GENE MUTATION, QUALITATIVE
This test identifies specific genetic variations (mutations) in the MTHFR gene, specifically C677T and A1298C. These mutations can affect how your body processes folate (Vitamin B9), which is vital for many bodily functions, including DNA synthesis and repair.
MTHFR (C677T) Mutation Analysis
This test specifically analyzes the C677T mutation in the MTHFR gene. This particular genetic variation can impact your body's ability to convert folate into its active form, which is crucial for various metabolic processes, including detoxification and neurotransmitter production.
Mucopolysaccharides (MPS) Type-I
This test screens for Mucopolysaccharidosis Type I (MPS I), a rare genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase. This enzyme is essential for breaking down complex sugars (mucopolysaccharides) in the body.
Mucopolysaccharides (MPS) Type-VI
This test screens for Mucopolysaccharidosis Type VI (MPS VI), also known as Maroteaux-Lamy syndrome. It's a rare genetic disorder caused by a deficiency in the enzyme N-acetylgalactosamine-4-sulfatase, which is vital for breaking down specific complex sugars.
Mucopolysaccharides (MPS) Typing
This test analyzes urine for specific types of mucopolysaccharides, which are complex sugar molecules. It helps identify and classify different forms of mucopolysaccharidosis, a group of rare genetic disorders.