MeSH Browser

MeSH Supplementary: Mental Retardation, X-Linked, Syndromic 10
Unique ID: C564560
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564560
Entry Term(s): 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency; 17beta-Hydroxysteroid Dehydrogenase Type 10 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; Chorioathetosis With Mental Retardation And Abnormal Behavior; HSD17B10 Deficiency; Hydroxyacyl-CoA Dehydrogenase II Deficiency; Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency; MRXS10; Mental Retardation With Chorioathetosis And Abnormal Behavior
Registry Number: 0
Heading Mapped to: *Dyskinesias; *Mental Retardation, X-Linked
Frequency: 6
Note: associated with hemizygous or heterozygous mutations in the HSD17B10 gene; OMIM: 300438
Date of Entry: 2012/11/05
Revision Date: 2017/10/19

Mental Retardation, X-Linked, Syndromic 10 MeSH Supplementary Concept Data 2023