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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Miraca Genetics Laboratories
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Medical Genetics Test Services

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   MAK-Related Retinitis Pigmentosa OMIM
   Malabsorptive Congenital Diarrhea 4 (NEUROG3) OMIM
   Maple Syrup Urine Disease (4 gene panel by NGS) GeneReview
   Maple Syrup Urine Disease Type 1A (BCKDHA) OMIM
   Maple Syrup Urine Disease Type 1B (BCKDHB) OMIM
   Maple Syrup Urine Disease Type 2 (DBT) OMIM GeneReview
   Maple Syrup Urine Disease Type 3 (DLD) OMIM
   MARS2 Related Disorders OMIM
   Maturity-Onset Diabetes of the Young (MODY) (25 gene panel by NGS)
   Maturity-onset Diabetes of the Young 6 (NEUROD1) OMIM
   Maturity-onset Diabetes of the Young, Type 11 (BLK) OMIM
   Maturity-onset Diabetes of the Young, Type VII (KLF11) OMIM
   MCAD Deficiency (ACADM) OMIM GeneReview
   MECP2 - Related Disorders OMIM GeneReview
   MEF2C - Related Disorders OMIM
   MEFV Related Disorders OMIM
   Megalencephalic Leukoencephalopathy with Subcortical Cysts OMIM
   Menkes Disease (ATP7A) OMIM GeneReview
   MERTK-Related Retinitis Pigmentosa OMIM
   MET Related Disorders OMIM
   Methylcobalamin Deficiency, cblG Type (MTR) OMIM
   Methylmalonic Acid - Plasma GeneReview
   Methylmalonic Acidemia - 3 Gene Panel (MUT, MMAA, MMAB)
   Methylmalonic Acidemia - MCEE Related OMIM GeneReview
   Methylmalonic Acidemia - MMAA Related (cblA) OMIM GeneReview
   Methylmalonic Acidemia - MMAB Related (cblB) OMIM GeneReview
   Methylmalonic Acidemia - MMADHC Related OMIM GeneReview
   Methylmalonic Acidemia - MUT Related OMIM GeneReview
   Methylmalonic Acidemia and Homocysteinemia, cblX Type (HCFC1) OMIM
   Methylmalonic Aciduria and Homocystinuria, cblJ Type (ABCD4) OMIM
   Methylmalonic Aciduria due to Transcobalamin Receptor Defect (CD320) OMIM
   MHC Class II Deficiency Complementation Group B (RFXANK) OMIM
   Microcephaly, Epilepsy, and Diabetes Syndrome (IER3IP1) OMIM
   Microphthalmia, Isolated 5 Disorder (MFRP) OMIM
   Microsatellite Instability Analysis (NCI Panel) OMIM GeneReview
   Mismatch Repair Proteins Immunohistochemistry
   Mitchell-Riley Syndrome (RFX6) OMIM
   Mitochondrial Complex I Deficiency - NDUFB8 Related OMIM
   Mitochondrial Complex I Deficiency-FOXRED1 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFA11 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFA2 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFA8 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFAF3 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFAF5 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFB6 Related OMIM
   Mitochondrial Complex I Deficiency-NDUFV3 Related OMIM
   Mitochondrial Complex I Deficiency-NUBPL Related OMIM
   Mitochondrial Complex II Deficiency, SDHAF1 Related OMIM
   Mitochondrial Complex III Deficiency-TTC19 Related OMIM
   Mitochondrial Complex III Deficiency-UQCRB Related OMIM
   Mitochondrial Complex III Deficiency-UQCRQ Related OMIM
   Mitochondrial Complex IV Deficiency-COX4I1 Related OMIM
   Mitochondrial Complex IV Deficiency-COX4I2 Related OMIM
   Mitochondrial Complex IV Deficiency-COX7A1 Related OMIM
   Mitochondrial Complex IV Deficiency-TACO1 Related OMIM
   Mitochondrial Complex V Deficiency-ATP5E Related OMIM
   Mitochondrial Complex V Deficiency-ATPAF2 Related (ATP12) OMIM
   Mitochondrial Depletion Syndrome Panel (20 gene panel by NGS)
   Mitochondrial DNA Content (qPCR) Analysis - Liver
   Mitochondrial DNA Content (qPCR) Analysis - Skeletal Muscle
   Mitochondrial DNA Depletion Syndrome 11 (MGME1) OMIM
   Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) (FBXL4) OMIM
   Mitochondrial DNA Depletion Syndrome SUCLG2-Related OMIM
   Mitochondrial DNA Point Mutations and Deletions-NGS
   Mitochondrial Genome Comprehensive Analysis
   Mitochondrial Myopathy and Sideroblastic Anemia Type 1 (PUS1) OMIM
   Mitochondrial Myopathy and Sideroblastic Anemia Type 2 (YARS2)
   Mitochondrial Nonsyndromic Hearing Loss and Deafness Mutation Panel OMIM GeneReview
   Mitochondrial Phosphate Carrier Deficiency (SLC25A3, PHC) OMIM
   Mitochondrial Respiratory Chain Complex I Deficiency (25 nuclear gene panel by NGS) OMIM
   Mitochondrial Respiratory Chain Complex II Deficiency (6 nuclear gene panel OMIM
   Mitochondrial Respiratory Chain Complex III Deficiency (4 nuclear gene panel by NGS) OMIM
   Mitochondrial Respiratory Chain Complex IV Deficiency (12 nuclear gene panel by NGS) OMIM
   Mitochondrial Respiratory Chain Complex I-V Deficiency (50 nuclear gene pan
   Mitochondrial Respiratory Chain Complex V Deficiency (3 nuclear gene panel by NGS)
   Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skeletal Muscle OMIM GeneReview
   Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skin Fibroblasts OMIM GeneReview
   Mitochondrial/Metabolic (MitoMetŪPlus) Microarray Analysis
   Mitochondrial/Metabolic (MitoMetŪPlus) Microarray Analysis
   Mitome200-Dual Genome Panel by NGS (201 gene panel by NGS)
   Mitome200-Nuclear Gene Panel by NGS (164 gene panel by NGS)
   MKKS Related Disorders OMIM
   MKS1 Related Disorders OMIM
   MMACHC (cblC) - Related Disorders OMIM GeneReview
   MNGIE Syndrome (TYMP or ECGF1) OMIM GeneReview
   Modifier of Bardet-Biedl syndrome (CCDC28B) OMIM
   MODY Type I (HNF4A) OMIM
   Molybdenum Cofactor Deficiency - MOCS1 Related OMIM
   Molybdenum Cofactor Deficiency - MOCS2 Related OMIM
   MPD Panel - JAK2V617F, JAK2 Exon 12, MPL Exon 10
   MPL Exon 10 Mutation Analysis OMIM
   MPL Related Disorders OMIM
   MPV17 - Related Disorders OMIM
   MPZ Related Disorders OMIM
   MRPL40 Related disorders OMIM
   MRPL44 Related disorders OMIM
   MRPS18A Related disorders OMIM
   MRPS2 Related disorders OMIM
   MRRF Related disorders OMIM
   MTFMT Related disorders OMIM
   MTHFR Thermolabile Variant Analysis OMIM
   MTRR Related Disorders OMIM GeneReview
   Mucolipidosis I [Sialidosis] OMIM
   Mucolipidosis IV OMIM
   Mucopolysaccharidisis Type IIIA (Sanfilippo A) OMIM
   Mucopolysaccharidosis Type I OMIM GeneReview
   Mucopolysaccharidosis Type II OMIM GeneReview
   Mucopolysaccharidosis Type IVA OMIM
   Mucopolysaccharidosis Type VI (ARSB) OMIM
   Multiple Acyl-CoA Dehydrogenase Deficiency - ETFA Related OMIM
   Multiple Acyl-CoA Dehydrogenase Deficiency - ETFB Related OMIM
   Multiple Acyl-CoA Dehydrogenase Deficiency - ETFDH Related OMIM
   Multiple Acyl-CoA Dehydrogenase Deficiency Panel (ETFA, ETFB & ETFDH)
   Multiple Endocrine Neoplasia Type 1 OMIM GeneReview
   Multiple Intestinal Atresia (TTC7A) OMIM
   Muscular Dystrophy (36 gene panel by NGS)
   Muscular Dystrophy-Dystroglycanopathy 9 (Limb-Girdle) Type C OMIM
   MUTYH (MYH) - Associated Polyposis OMIM
   MYBPC3 Related Disorders OMIM
   MYH7 Related Disorders OMIM
   MYO7A - Related Disorders OMIM
   Myoclonic Dystonia-11 OMIM
   Myopathy due to Myoadenylate Deaminase Deficiency OMIM
   Myopathy with Deficiency of ISCU OMIM GeneReview
   Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay (GFER) OMIM
   Myopathy/Rhabdomyolysis Panel by NGS (27 gene panel by NGS)
   MYOT Related Disorders OMIM
   Myotonic Dystrophy Type 1 OMIM GeneReview