Clinical and research tests for 1-Methyl-1-phenylthiourea - Genetic Testing Registry (GTR)

Results: 1 to 3 of 3

Select all conditions on this page	Conditions	Synonyms
Select item 82784	Corticosterone 18-monooxygenase deficiency	18 Hydroxylase deficiency 18 alpha hydroxylase deficiency ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE ALDOSTERONE DEFICIENCY I Aldosterone deficiency 1 Aldosterone deficiency due to defect in 18 hydroxylase CMO 1 deficiency CMO I DEFICIENCY Corticosterone methyloxidase type 1 deficiency STEROID 18-HYDROXYLASE DEFICIENCY
Select item 78692	Deficiency of hydroxymethylglutaryl-CoA lyase	3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency 3-hydroxy-3-methylglutaric aciduria Defect in leucine metabolism HMG CoA lyase deficiency HMGCL DEFICIENCY Hydroxymethylglutaric aciduria
Select item 483046	Corticosterone methyloxidase type 2 deficiency	18-OXIDASE DEFICIENCY ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE ALDOSTERONE DEFICIENCY II CMO II DEFICIENCY Corticosterone Methyloxidase Type II Deficiency STEROID 18-OXIDASE DEFICIENCY

Results: 1 to 3 of 3

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