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Mental Retardation, X-Linked, Syndromic 10 [Supplementary Concept]

associated with hemizygous or heterozygous mutations in the HSD17B10 gene; OMIM: 300438

Date introduced: November 5, 2012

MeSH Unique ID: C564560

Heading Mapped to:

Entry Terms:

  • Mental Retardation With Chorioathetosis And Abnormal Behavior
  • MRXS10
  • Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency
  • 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency
  • Hydroxyacyl-CoA Dehydrogenase II Deficiency
  • 2-Methyl-3-Hydroxybutyric Aciduria
  • 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency
  • 3-Hydroxy-2-Methylbutyryl-CoA Dehydrogenase Deficiency
  • 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
  • 3-Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency
  • HSD17B10 Deficiency
  • Chorioathetosis With Mental Retardation And Abnormal Behavior
  • 17beta-Hydroxysteroid Dehydrogenase Type 10 Deficiency

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