Clinical and research tests for Methionine synthase - Genetic Testing Registry (GTR)

Results: 1 to 5 of 5

Select all conditions on this page	Conditions	Synonyms
Select item 344426	Methylcobalamin deficiency type cblG Tests Gene GeneReviews	Functional methionine synthase deficiency type cblG HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblG COMPLEMENTATION TYPE HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblG COMPLEMENTATION TYPE
Select item 766829	Methylmalonic acidemia with homocystinuria, type cblJ Tests Gene GeneReviews	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE
Select item 929148	Homocystinuria without methylmalonic aciduria Tests Genes GeneReviews
Select item 344640	Methylcobalamin deficiency type cblE Tests Gene GeneReviews	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type VITAMIN B12-RESPONSIVE HOMOCYSTINURIA, cblE TYPE
Select item 1826168	Methylcobalamin deficiency type cblDv1 Tests Genes GeneReviews

Results: 1 to 5 of 5

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