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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:X-linked mental retardation Gustavson type
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Accession:DOID:0081123 term browser browse the term
Definition:A syndromic X-linked intellectual disability that is characterized by severe intellectual disability, microcephaly, post-natal growth retardation, severe visual impairment or blindness, severe hearing defect, spasticity, epileptic seizures, restricted large-joint movements and early death. (DO)
Synonyms:exact_synonym: GUST;   Gustavson syndrome;   MRXSG;   Mental retardation X-linked severe Gustavson type;   Mental retardation with optic atrophy, deafness, and seizures;   intellectual developmental disorder with optic atrophy, deafness, and seizures;   intellectual developmental disorder, X-linked syndromic, Gustavson type
 primary_id: MESH:C536759
 alt_id: DOID:9000015;   MIM:309555
 xref: GARD:5611;   ORDO:3078


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X-linked mental retardation Gustavson type term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G RBMX RNA binding motif protein X-linked ISO ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES | ClinVar Annotator: match by term: Mental retardation Gustavson type, X-linked OMIM
ClinVar		 PMID:25741868 NCBI chr  X:107,173,599...107,182,404
Ensembl chr  X:107,175,634...107,182,347 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15673
    Pathological Conditions, Signs and Symptoms 12220
      Anatomical Pathological Conditions 2579
        Atrophy 361
          optic atrophy 191
            X-linked mental retardation Gustavson type 1
Path 2
Term Annotations click to browse term
  disease 15673
    disease of anatomical entity 15313
      nervous system disease 13402
        central nervous system disease 12030
          brain disease 11302
            disease of mental health 8173
              developmental disorder of mental health 5593
                specific developmental disorder 4561
                  intellectual disability 4364
                    X-Linked Intellectual Developmental Disorders 819
                      syndromic X-linked intellectual disability 623
                        X-linked mental retardation Gustavson type 1
paths to the root