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Results 1 - 10 of 17 for Hydroxysteroid
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  1. 3-beta (β)-hydroxysteroid dehydrogenase (HSD) deficiency is an inherited disorder that affects hormone-producing glands including the gonads (ovaries in females ...
  2. 17-beta hydroxysteroid dehydrogenase 3 deficiency is a condition that affects male sexual development. People with this condition are genetically male, ...
  3. ... a role in causing intellectual disability. 17-beta-hydroxysteroid dehydrogenase type 10 17β-HSD10 2-methyl-3- ... binding alcohol dehydrogenase CAMR ERAB HADH2 HCD2 HSD10 hydroxysteroid (17-beta) dehydrogenase 10 MHBD MRPP2 SCHAD SDR5C1 ...
  4. ... instructions for making an enzyme called 17-beta hydroxysteroid dehydrogenase 3. This enzyme is active in the ... More than 20 mutations that cause 17-beta hydroxysteroid dehydrogenase 3 deficiency have been identified in the ...
  5. ... gene provides instructions for making the 3-beta-hydroxysteroid dehydrogenase (3β-HSD) enzyme. This enzyme is found ... Condition 3 beta-HSD type II 3 beta-hydroxysteroid dehydrogenase 2 3 beta-hydroxysteroid dehydrogenase type II, ...
  6. ... provides instructions for making an enzyme called 3β-hydroxysteroid-Δ8,Δ7-isomerase. This enzyme is responsible for ... protein building blocks (amino acids) in the 3β-hydroxysteroid-Δ8,Δ7-isomerase enzyme. All of these mutations ...
  7. ... HSD 4 17-beta-HSD IV 17-beta-hydroxysteroid dehydrogenase 4 17beta-estradiol dehydrogenase type IV 3- ... hydroxyacyl-CoA dehydratase D-bifunctional protein, peroxisomal DBP hydroxysteroid (17-beta) dehydrogenase 4 MFE-2 MPF-2 ...
  8. ... instructions for making an enzyme called 3 beta-hydroxysteroid dehydrogenase type 7 (3β-HSD7). This enzyme is ... hydroxy-delta 5-C27-steroid oxidoreductase 3 beta-hydroxysteroid dehydrogenase type 7 3 beta-hydroxysteroid dehydrogenase type ...
  9. ... pass X-linked traits to their sons. 17β-hydroxysteroid dehydrogenase type 10 deficiency 2-methyl-3-hydroxybutyric ... Zschocke J. Mutation or knock-down of 17beta-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and ...
  10. ... signs and symptoms of the condition. 17-beta-hydroxysteroid dehydrogenase IV deficiency Bifunctional peroxisomal enzyme deficiency DBP ... Specific combination of compound heterozygous mutations in 17beta-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype ...
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