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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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   LAMA2 Related Disorders OMIM
   LAMA3 Related Disorders OMIM
   LAMB2 Related Disorders OMIM
   LAMB3 Related Disorders OMIM
   LAMC2 Related Disorders OMIM
   LARGE Related Disorders OMIM
   LARS2-Related Disorders
   LCA5-Related Leber Congenital Amaurosis OMIM
   LCAD Deficiency (ACADL) OMIM
   LDB3 Related Disorders OMIM
   Leber Congenital Amaurosis Panel (19 gene panel by NGS)
   Leber Congenital Amaurosis, Calcium Binding Protein 4 Deficiency (CABP4) OMIM GeneReview
   Leber Congenital Amaurosis, IQ Motif Containing B1 Deficiency (IQCB1) OMIM GeneReview
   Leber Congenital Amaurosis, Nicotinamide Nucleotide Adenylyltransferase 1 Deficiency (NMNAT1) OMIM GeneReview
   Leber Congenital Amaurosis, Orthodenticle Homeobox 2 Deficiency (OTX2) OMIM
   Leber Congenital Amaurosis, Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 Deficiency (KCNJ13) OMIM GeneReview
   Leigh Disease (91 gene panel by NGS) GeneReview
   Leigh Syndrome - LRPPRC OMIM
   Lesch-Nyhan Syndrome OMIM GeneReview
   Leukemia Mutation Panel
   Leukoencephalopathy (DARS2) OMIM GeneReview
   Leukoencephalopathy with dystonia and motor neuropathy (SCP2) OMIM
   Li-Fraumeni Syndrome OMIM GeneReview
   LIG4 Related Disorders OMIM
   Limb-Girdle Muscular Dystrophy Type 1E OMIM
   Limb-Girdle Muscular Dystrophy Type 1F OMIM
   Limb-Girdle Muscular Dystrophy Type 2A OMIM
   Limb-Girdle Muscular Dystrophy Type 2C OMIM
   Limb-Girdle Muscular Dystrophy Type 2D OMIM
   Limb-Girdle Muscular Dystrophy Type 2E OMIM
   Limb-Girdle Muscular Dystrophy Type 2S OMIM
   Liver Failure, Acute Infantile (TRMU) OMIM
   LMBRD1 (cblF)-Related Disorders OMIM GeneReview
   LMNA Related Disorders OMIM
   Low Bone Mass Panel by NGS (23 gene panel by NGS)
   Lowe Syndrome OMIM GeneReview
   LRAT-Related Retinitis Pigmentosa OMIM
   LRP5 Related Disorders OMIM
   Lymphoproliferative Syndrome 1 (ITK) OMIM
   Lymphoproliferative Syndrome 1 X-linked (SH2D1A) OMIM
   Lysinuric Protein Intolerance OMIM