U.S. flag

An official website of the United States government

GTR Home > Laboratories > Diagnostics Division

Diagnostics Division

GTR Lab ID: 505641, Last updated:2021-11-15
Annual Review past due read more

Personnel

  • Director: Ashwin Dalal, MD, Lab Director
    Phone: +91-40-24749338,339
    Fax: +91-40-24749448
    Email: nidaan@cdfd.org.in

Conditions and tests

  • 46,XY difference of sex development due to a defect in testosterone metabolism by peripheral tissue1 test
  • Achondroplasia1 test
  • Advanced maternal age1 test
  • Alkaptonuria1 test
  • Alopecia - intellectual disability syndrome1 test
  • alpha Thalassemia1 test
  • Aminoaciduria1 test
  • Anemia2 tests
  • Aneuploidy, chromosomal rearrangements, chromosomal deletion, chromosomal duplication1 test
  • Autosomal chromosomal disorder1 test
  • Autosomal recessive distal spinal muscular atrophy 12 tests
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Autosomal recessive nonsyndromic hearing loss 1B1 test
  • Azorean disease1 test
  • Becker muscular dystrophy1 test
  • beta Thalassemia2 tests
  • Beta thalassemia intermedia2 tests
  • Beta-thalassemia major2 tests
  • Biotinidase deficiency1 test
  • Chromosome 3, trisomy 3p1 test
  • Chromosome 5, trisomy 5p1 test
  • Complete trisomy 13 syndrome1 test
  • Complete trisomy 20 syndrome1 test
  • Complete trisomy 21 syndrome1 test
  • Congenital chromosomal disease2 tests
  • Congenital muscular dystrophy1 test
  • Congenital prothrombin deficiency1 test
  • Cystic fibrosis1 test
  • Deafness, digenic, GJB2/GJB61 test
  • Deficiency of alpha-mannosidase1 test
  • Dentatorubral-pallidoluysian atrophy1 test
  • Distal spinal muscular atrophy1 test
  • Duchenne / Becker Muscular Dystrophy1 test
  • Duchenne muscular dystrophy1 test
  • Dysmorphism-short stature-deafness-disorder of sex development syndrome1 test
  • Fabry disease1 test
  • Factor V deficiency1 test
  • Fragile X syndrome1 test
  • Fragile X-associated tremor/ataxia syndrome1 test
  • Friedreich ataxia1 test
  • Friedreich ataxia 11 test
  • Friedreich ataxia 21 test
  • Fucosidosis2 tests
  • Galactosemia1 test
  • Galactosylceramide beta-galactosidase deficiency1 test
  • Gaucher disease1 test
  • Gilbert syndrome, susceptibility to1 test
  • Glycogen storage disease, type II1 test
  • GM1 gangliosidosis1 test
  • Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy1 test
  • Hb SS disease2 tests
  • Hemoglobinopathy2 tests
  • Hemophilia1 test
  • Hereditary pancreatitis1 test
  • Homocystinuria due to methylene tetrahydrofolate reductase deficiency1 test
  • Huntington disease1 test
  • Hurler syndrome1 test
  • Hyperhomocysteinemia2 tests
  • Infertility disorder1 test
  • Intellectual disability1 test
  • Intrauterine growth retardation with increased mitomycin c sensitivity1 test
  • Kennedy disease1 test
  • Klinefelter syndrome1 test
  • Leber optic atrophy1 test
  • Metachromatic leukodystrophy1 test
  • Mild hemophilia A1 test
  • Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
  • Morquio syndrome2 tests
  • Mucopolysaccharidosis1 test
  • Mucopolysaccharidosis type 12 tests
  • Mucopolysaccharidosis type 61 test
  • Mucopolysaccharidosis type 71 test
  • Mucopolysaccharidosis, MPS-I-H/S1 test
  • Mucopolysaccharidosis, MPS-I-S1 test
  • Mucopolysaccharidosis, MPS-II1 test
  • Mucopolysaccharidosis, MPS-IV-A1 test
  • Mucopolysaccharidosis, MPS-IV-B1 test
  • Neurodevelopmental disorder with alopecia and brain abnormalities1 test
  • Niemann-Pick disease, type A1 test
  • Niemann-Pick disease, type B1 test
  • Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive1 test
  • Phenylketonuria1 test
  • PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome1 test
  • Pregnancy loss, recurrent, susceptibility to, 11 test
  • Qualitative or quantitative defects of dystrophin1 test
  • Sandhoff disease1 test
  • Sanfilippo syndrome1 test
  • Severe hemophilia A2 tests
  • Sex-linked hereditary disorder1 test
  • Sickle cell-beta-thalassemia2 tests
  • Sickle cell-hemoglobin C disease1 test
  • Sickle cell-hemoglobin D disease1 test
  • Sickle cell-Hemoglobin O Arab disease1 test
  • Spinocerebellar ataxia type 11 test
  • Steinert myotonic dystrophy syndrome1 test
  • Symptomatic form of hemophilia A in female carriers1 test
  • Tay-Sachs disease1 test
  • Thakker-Donnai syndrome1 test
  • Thalassemia2 tests
  • Thalassemia intermedia2 tests
  • Thalassemia minor2 tests
  • Triploidy and tetraploidy1 test
  • Trisomy 181 test
  • trisomy 21, 18 and 131 test
  • Trisomy 81 test
  • Turner syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Confirmation of research findings
  • Prenatal testing
  • Genetic counseling
  • Maternal cell contamination study (MCC)
  • Mutation Confirmation
  • Result interpretation

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.