Molecular Diagnostic Laboratory (Diagnostic Services, Shared Health Manitoba)
General information
Molecular Diagnostic Laboratory
Diagnostic Services, Shared Health Manitoba
820 Sherbrook Street, RmMS471A
Winnipeg
Manitoba
Canada - R3L1R9
https://apps.sbgh.mb.ca/labmanual/test/findTestPrepare
Organization ID: 1070
Diagnostic Services, Shared Health Manitoba
820 Sherbrook Street, RmMS471A
Winnipeg
Manitoba
Canada - R3L1R9
https://apps.sbgh.mb.ca/labmanual/test/findTestPrepare
Organization ID: 1070
Personnel
- Ronald Agatep, Lab Director
Phone: 2047872845
Email: ragatep@sharedhealthmb.ca - Assaf Sheffer, Informatics staff
Phone: 972547494850
Email: adaia@genoox.com - Elizabeth Spriggs, Lab Director
Phone: 2047872843
Email: bspriggs@sharedhealthmb.ca
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 2
Condition
Name | Submissions | Last Updated |
---|---|---|
Sialic acid storage disease, severe infantile type | 1 | Sep 23, 2021 |
Sulfite oxidase deficiency | 1 | Dec 12, 2020 |
Testing in GTR
Disease name | Number of tests |
---|---|
Angelman syndrome | 1 test |
Autosomal recessive nonsyndromic hearing loss 1A | 1 test |
Azorean disease | 1 test |
Charcot-Marie-Tooth disease, type IA | 1 test |
Congenital bilateral aplasia of vas deferens from CFTR mutation | 1 test |
Cystic fibrosis | 1 test |
Disorder of cardiovascular system | 1 test |
Disseminated bronchiectasis | 1 test |
Fragile X syndrome | 1 test |
Fragile X-associated tremor/ataxia syndrome | 1 test |
Hemochromatosis type 1 | 1 test |
Hereditary liability to pressure palsies | 1 test |
Huntington disease | 1 test |
Hypophosphatasia | 1 test |
Kennedy disease | 1 test |
Oculopharyngeal muscular dystrophy | 1 test |
Prader-Willi syndrome | 1 test |
Premature ovarian failure 1 | 1 test |
Recurrent acute pancreatitis | 1 test |
Spermatogenic failure, Y-linked, 2 | 1 test |
Spinocerebellar ataxia 7 | 1 test |
Spinocerebellar ataxia type 1 | 1 test |
Spinocerebellar ataxia type 2 | 1 test |
Spinocerebellar ataxia type 6 | 1 test |
Spinocerebellar ataxia type 8 | 1 test |
Steinert myotonic dystrophy syndrome | 1 test |
chronic recurrent pancreatitis | 1 test |