Molecular Genetics Diagnostic Laboratory (Detroit Medical Center University Laboratories)
General information
Molecular Genetics Diagnostic Laboratory
Detroit Medical Center University Laboratories
WG71 Hutzel Building
4707 St. Antoine
Detroit
Michigan
United States - 48201
https://www.dmc.org/health-professionals/university-labs
Organization ID: 1167
Detroit Medical Center University Laboratories
WG71 Hutzel Building
4707 St. Antoine
Detroit
Michigan
United States - 48201
https://www.dmc.org/health-professionals/university-labs
Organization ID: 1167
Personnel
- Fatimah Nahhas
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 8
Gene
Gene | Submissions | Last Updated |
---|---|---|
BTD | 8 | Aug 13, 2014 |
Condition
Name | Submissions | Last Updated |
---|---|---|
Biotinidase deficiency | 8 | Aug 13, 2014 |
Testing in GTR
Disease name | Number of tests |
---|---|
Acquired polycythemia vera | 2 tests |
Acute lymphoid leukemia | 1 test |
Acute myeloid leukemia | 4 tests |
Alpha trait thalassemia | 1 test |
Beta thalassemia intermedia | 1 test |
Beta-thalassemia major | 1 test |
Carcinoma of colon | 2 tests |
Cetuximab response | 3 tests |
Chronic myelogenous leukemia, BCR-ABL1 positive | 1 test |
EGFR-related lung cancer | 1 test |
Erlotinib response | 1 test |
Essential thrombocythemia | 1 test |
Fragile X syndrome | 1 test |
Fragile X-associated tremor/ataxia syndrome | 1 test |
Gastrointestinal stromal tumor | 1 test |
Gefitinib response | 1 test |
Gilbert syndrome | 1 test |
Hairy cell leukemia | 1 test |
Hb SS disease | 2 tests |
Hemochromatosis type 1 | 1 test |
Hemoglobin Bart hydrops syndrome | 1 test |
Hemoglobin H disease | 1 test |
Hereditary hemochromatosis | 1 test |
Homocystinuria due to methylene tetrahydrofolate reductase deficiency | 1 test |
Huntington disease | 1 test |
Irinotecan response | 1 test |
Juvenile Huntington disease | 1 test |
Langerhans cell histiocytosis | 1 test |
Lymphoma | 2 tests |
Lynch syndrome | 1 test |
MTHFR THERMOLABILE POLYMORPHISM | 1 test |
Mastocytosis | 1 test |
Melanoma | 1 test |
Myelodysplastic syndrome | 1 test |
Myeloproliferative disorder | 3 tests |
Panitumumab response | 1 test |
Premature ovarian failure 1 | 1 test |
Primary myelofibrosis | 2 tests |
Sickle cell-Hemoglobin O Arab disease | 1 test |
Sickle cell-beta-thalassemia | 1 test |
Sickle cell-hemoglobin C disease | 2 tests |
Sickle cell-hemoglobin D disease | 1 test |
Thalassemia minor | 1 test |
Thiopurine S-methyltransferase deficiency | 1 test |
Thrombocythemia 1 | 1 test |
Thrombophilia | 1 test |
Thrombophilia due to activated protein C resistance | 1 test |
Transcription level of plasminogen activator inhibitor 1 | 1 test |
Tyrosine kinase inhibitor response | 2 tests |
Vemurafenib response | 1 test |
alpha Thalassemia | 1 test |
beta Thalassemia | 1 test |
methotrexate response - Toxicity | 1 test |