Genome-Nilou Lab

Personnel

Director: Mohammad Hossein Modarressi, PhD, MD, Lab Director
Director: Shahram Savad, PhD, MD, Lab Director
Mostafa Iranpour, Administrator
Email: shahram.savad@yahoo.com

Conditions and tests

157 conditions/phenotypes with 4 tests
Enter text to narrow down the list

3 beta-Hydroxysteroid dehydrogenase deficiency1 test
3-Methylglutaconic aciduria1 test
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency1 test
Abetalipoproteinaemia1 test
Acquired polycythemia vera1 test
Acute myeloid leukemia1 test
Adenomatous polyposis coli, attenuated1 test
Adrenal cortex carcinoma1 test
Adrenoleukodystrophy1 test
Alpha-thalassemia/intellectual disability syndrome1 test
Alport syndrome1 test
Alstrom syndrome1 test
Aneuploidy1 test
Argininosuccinate lyase deficiency1 test
Aromatase deficiency1 test
Ataxia-telangiectasia syndrome1 test
Autosomal recessive polycystic kidney disease1 test
B-cell non-Hodgkin lymphoma1 test
Bardet-Biedl syndrome1 test
Basal cell carcinoma1 test
beta Thalassemia1 test
Biotinidase deficiency1 test
Bloom syndrome1 test
Breast adenocarcinoma1 test
Canavan Disease, Familial Form1 test
Capillary infantile hemangioma1 test
Carcinoma of colon1 test
Carcinoma of pancreas1 test
Carnitine palmitoyl transferase 1A deficiency1 test
Carnitine palmitoyltransferase II deficiency1 test
Carpenter syndrome1 test
Charcot-Marie-Tooth disease type 51 test
Charlevoix-Saguenay spastic ataxia1 test
Chronic granulomatous disease1 test
Citrin deficiency1 test
Citrullinemia type I1 test
Cobalamin C disease1 test
Cohen syndrome1 test
Combined malonic and methylmalonic acidemia1 test
Congenital adrenal hyperplasia1 test
Congenital amegakaryocytic thrombocytopenia1 test
Congenital lipoid adrenal hyperplasia due to STAR deficency1 test
Corticosterone methyloxidase type 2 deficiency1 test
Cystic fibrosis1 test
Deficiency of acetyl-CoA acetyltransferase1 test
Deficiency of alpha-mannosidase1 test
Deficiency of galactokinase1 test
Deficiency of hydroxymethylglutaryl-CoA lyase1 test
Disorder of fructose metabolism1 test
Duchenne muscular dystrophy1 test
Ellis-van Creveld syndrome1 test
Endometrial carcinoma1 test
Fabry disease1 test
Familial dysautonomia1 test
Familial hypercholesterolemia1 test
Familial hyperinsulinism1 test
Familial Mediterranean fever1 test
Fanconi anemia1 test
Follicular thyroid carcinoma1 test
Fumarase deficiency1 test
Galactosemia1 test
Galactosylceramide beta-galactosidase deficiency1 test
Gastric cancer1 test
Gastrointestinal stromal tumor1 test
Gaucher disease1 test
Glioblastoma1 test
Glioma1 test
Glutaric acidemia IIa1 test
Glutaric acidemia IIc1 test
Glutaric aciduria, type 11 test
Glycogen storage disease1 test
GRACILE syndrome1 test
Hemangioblastoma1 test
Hemochromatosis type 2A1 test
Hepatic adenomas, familial1 test
Hepatoblastoma1 test
Hepatocellular carcinoma1 test
Hereditary factor IX deficiency disease1 test
Hereditary insensitivity to pain with anhidrosis1 test
Holocarboxylase synthetase deficiency1 test
Homocystinuria1 test
Hyperlipoproteinemia1 test
Hypohidrotic ectodermal dysplasia1 test
Hypophosphatasia1 test
Isovaleric acidemia, type I1 test
Juvenile myelomonocytic leukemia1 test
Leber congenital amaurosis1 test
Leukemia, Philadelphia chromosome-positive, resistant to imatinib1 test
Li-Fraumeni syndrome1 test
Limb-girdle muscular dystrophy1 test
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency1 test
Lung carcinoma1 test
Malignant melanoma of skin1 test
Malignant tumor of testis1 test
Mantle cell lymphoma1 test
Maple syrup urine disease1 test
Meckel syndrome, type 11 test
Medium chain 3-ketoacyl-Coa thiolase deficiency1 test
Medullary thyroid carcinoma1 test
Medulloblastoma1 test
Megalencephalic leukoencephalopathy with subcortical cysts1 test
Meningioma1 test
Menkes kinky-hair syndrome1 test
Metabolic disease1 test
Metachromatic leukodystrophy1 test
Methylcrotonyl-CoA carboxylase deficiency1 test
Methylmalonic acidemia1 test
Mitochondrial complex I deficiency1 test
Mucolipidosis1 test
Mucopolysaccharidosis1 test
Multiple sulfatase deficiency1 test
Muscle eye brain disease1 test
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A11 test
Nasopharyngeal carcinoma1 test
Nephrotic syndrome1 test
Neuroblastoma1 test
Niemann-Pick disease, type A1 test
Niemann-Pick disease, type B1 test
Niemann-Pick disease, type C1 test
Nijmegen breakage syndrome-like disorder1 test
Non-small cell lung carcinoma1 test
Nonsyndromic genetic hearing loss1 test
Ornithine carbamoyltransferase deficiency1 test
Osteosarcoma1 test
Ovarian adenocarcinoma1 test
Pendred syndrome1 test
Periampullary adenoma1 test
Phenylketonuria1 test
Pituitary adenoma 3, multiple types1 test
Primary ciliary dyskinesia1 test
Primary myelofibrosis1 test
Propionic acidemia1 test
Prostate cancer susceptibility1 test
Pyruvate dehydrogenase complex deficiency1 test
Pyruvate dehydrogenase E1-alpha deficiency1 test
Pyruvate dehydrogenase E1-beta deficiency1 test
Renal carnitine transport defect1 test
Renal cell carcinoma1 test
Retinitis pigmentosa 251 test
Retinoblastoma1 test
Rhabdoid tumors, somatic1 test
Schwannomatosis1 test
Severe combined immunodeficiency disease1 test
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency1 test
Smith-Lemli-Opitz syndrome1 test
Sulfate transporter-related osteochondrodysplasia1 test
T-cell prolymphocytic leukemia1 test
Tay-Sachs disease1 test
Tyrosinemia type I1 test
Urinary bladder carcinoma1 test
Usher syndrome1 test
Vanishing white matter disease1 test
Very long chain acyl-CoA dehydrogenase deficiency1 test
Wilson disease1 test
X-linked Emery-Dreifuss muscular dystrophy1 test
X-linked severe combined immunodeficiency1 test
Zellweger spectrum disorders1 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously
Custom Deletion/Duplication Testing
Prenatal testing
Carrier testing
Genetic counseling
Identity Testing
Mutation Confirmation
Whole Exome Sequencing
Whole Genome Sequencing

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.