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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:syndromic X-linked intellectual disability type 10
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Accession:DOID:0060810 term browser browse the term
Definition:A syndromic X-linked intellectual disability characterized by mild intellectual deficit associated with choreoathetosis and abnormal behaviour that has_material_basis_in mutation in the HSD17B10 gene on chromosome Xp11.22. (DO)
Synonyms:exact_synonym: 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;   CAMR;   Chorioathetosis With Mental Retardation And Abnormal Behavior;   HSD10 MITOCHONDRIAL DISEASE;   HSD10 deficiency, atypical type;   HSD10 disease, atypical type;   HSD10MD;   HSD17B10 Deficiency;   HSD17B10-RELATED DISORDER;   Hydroxyacyl-CoA Dehydrogenase II Deficiency;   MHBD deficiency;   MRXS10;   X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome;   hydroxyacyl-CoA dehydrogenase type 2 deficiency;   syndromic X-linked mental retardation 10
 primary_id: MESH:C564560
 alt_id: MIM:300438
 xref: ICD10CM:G25.5;   ORDO:85295


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syndromic X-linked intellectual disability type 10 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Hsd17b10 hydroxysteroid (17-beta) dehydrogenase 10 ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: CHORIOATHETOSIS WITH MENTAL RETARDATION AND ABNORMAL BEHAVIOR | ClinVar Annotator: match by term: HSD10 mitochondrial disease | ClinVar Annotator: match by term: HSD17B10-related disorder		 OMIM
CTD
ClinVar		 PMID:10521307 PMID:11102558 PMID:12112118 PMID:12555940 PMID:12696021 More... NCBI chr  X:21,089,142...21,091,603
Ensembl chr  X:21,089,122...21,109,488 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19102
    Nutritional and Metabolic Diseases 8520
      disease of metabolism 8520
        lipid metabolism disorder 1901
          syndromic X-linked intellectual disability type 10 1
Path 2
Term Annotations click to browse term
  disease 19102
    disease of anatomical entity 18443
      nervous system disease 14336
        central nervous system disease 12608
          brain disease 11837
            disease of mental health 8428
              developmental disorder of mental health 5649
                specific developmental disorder 4605
                  intellectual disability 4384
                    X-Linked Intellectual Developmental Disorders 824
                      syndromic X-linked intellectual disability 620
                        syndromic X-linked intellectual disability type 10 1
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