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Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
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Medical Genetics Test Services

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  Paget Disease, Juvenile (TNFRSF11B) OMIM
  Paraganglioma/Pheochromocytoma (TMEM127) OMIM
  PAX4 Related Disorders OMIM
  PAX6 Related Disorders OMIM
  PCDH19 - Related X-Linked Female-Limited Epilepsy w/MR OMIM
  PDE6A-Related Retinitis Pigmentosa OMIM
  PDE6B-Related Retinitis Pigmentosa OMIM
  PDE6G-Related Retinitis Pigmentosa OMIM
  PDH & Mitochondrial Respiratory Chain Complex V Deficiency (9 nuclear gene panel by NGS)
  PDHA1 - Related Disorders OMIM
  PDX1 Related Disorders OMIM
  Pelizaeus-Merzbacher-Like Disease OMIM
  PEPCK deficiency, mitochondrial (PCK2) OMIM
  Permanent Neonatal Diabetes Mellitus with Cerebellar Agenesis (PTF1A) OMIM
  Peroxisomal acyl-CoA oxidase deficiency (ACOX1) OMIM
  Peroxisomal Disorders (22 gene panel by NGS) GeneReview
  Peroxisome Biogenesis Disorder 1 (PEX1) OMIM
  Peroxisome Biogenesis Disorder 10A (Zellweger) (PEX3) OMIM
  Peroxisome Biogenesis Disorder 11 (PEX13) OMIM
  Peroxisome Biogenesis Disorder 12A (Zellweger) (PEX19) OMIM
  Peroxisome Biogenesis Disorder 13A (Zellweger) (PEX14) OMIM
  Peroxisome Biogenesis Disorder 14B (PEX11B) OMIM
  Peroxisome Biogenesis Disorder 2 (PEX5) OMIM
  Peroxisome Biogenesis Disorder 3 (PEX12) OMIM
  Peroxisome Biogenesis Disorder 4 (PEX6) OMIM
  Peroxisome Biogenesis Disorder 5 (PEX2) OMIM
  Peroxisome Biogenesis Disorder 6 (PEX10) OMIM
  Peroxisome Biogenesis Disorder 7 (PEX26) OMIM
  Peroxisome Biogenesis Disorder 8 (PEX16) OMIM
  PEX7 Related Disorders (PEX7) OMIM
  Phenylalanine Determination - Blood Spot OMIM GeneReview
  Phenylalanine Determination - Plasma OMIM GeneReview
  Phenylalanine Hydroxylase Deficiency (PAH) OMIM GeneReview
  Phenylbutyrate Metabolite Analysis
  PHEO and PGL Syndrome Panel (SDHB, SDHC, & SDHD) OMIM GeneReview
  Phosphoenolpyruvate carboxykinase-1, cytosolic, deficiency (PCK1) OMIM
  PHOX2B Related Disorders OMIM
  PIK3CA Mutation Analysis - Germline OMIM
  PIK3CA Mutation Analysis - Tumor OMIM
  PITX2 Related Disorders OMIM
  PITX3 Related Disorders OMIM
  PLOD3 Related Disorders OMIM
  PLP1 - Related Disorders OMIM GeneReview
  PML/RARA Transcripts for Promyelocytic Leukemia
  PMS2 Immunohistochemistry
  POLG - Related Disorders (POLG1, POLGA) OMIM GeneReview
  POLG2 - Related Disorders OMIM
  Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Disorder (ABHD12) OMIM
  Polyols - Urine
  Pontocerebellar Hypoplasia Type 6 (RARS2) OMIM
  PPIB-Related Osteogenesis Imperfecta OMIM
  Prader-Willi Syndrome OMIM GeneReview
  Prader-Willi-like Syndrome; Intellectual Disability; Autism (MAGEL2)
  PRCD-Related Retinitis Pigmentosa OMIM
  PRF1 Related Disorders OMIM
  Primary Open Angle Glaucoma (2 gene panel by NGS)
  Primary Open Angle Glaucoma 1A OMIM
  PRKAR1A Related Disorders OMIM
  PRKDC Related Disorders OMIM
  Progressive External Ophthalmoplegia - PEO Panel (10 gene panel by NGS)
  PROM1-Related Retinitis Pigmentosa OMIM
  Propionic Acidemia - PCCA Related OMIM GeneReview
  Propionic Acidemia - PCCB Related OMIM GeneReview
  Propionic Acidemia Panel (PCCA & PCCB)
  Prothrombin Mutation Panel OMIM GeneReview
  Proximal Urea Cycle Disorders (3 gene panel by NGS) GeneReview
  PRPF31-Related Retinitis Pigmentosa OMIM
  PRPF3-Related Retinitis Pigmentosa OMIM
  PRPF6-Related Retinitis Pigmentosa OMIM
  PRPF8-Related Retinitis Pigmentosa OMIM
  PRPH2-Related Retinitis Pigmentosa OMIM
  PTCH1 Related Disorders OMIM
  PTEN - Related Disorders OMIM
  PTPN11 - Related Disorders OMIM
  Purine and Pyrimidine Panel - Urine
  Purine Nucleoside Phosphorylase Deficiency (PNP) OMIM
  Purine Panel - Urine
  Pycnodysostosis (CTSK) OMIM
  Pyridoxine-Dependent Seizures OMIM GeneReview
  Pyrimidine Panel - Urine
  Pyruvate Carboxylase Deficiency (PC) OMIM GeneReview
  Pyruvate Dehydrogenase Deficiency (PDHB) OMIM
  Pyruvate Dehydrogenase E2 Deficiency (DLAT) OMIM
  Pyruvate Dehydrogenase E3-Binding Protein (Component X) Deficiency (PDHX) OMIM
  Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1) OMIM