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RGD uses the Human Disease Ontology (DO, 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:Wiedemann Oldigs Oppermann Syndrome
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Accession:DOID:9003592 term browser browse the term
Definition:A rare syndrome characterized mainly by excessive hair growth, mental retardation and skeletal abnormalities.
Synonyms:exact_synonym: hirsutism, skeletal dysplasia, mental retardation syndrome
 primary_id: MESH:C536705
 alt_id: RDO:0002363
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18145
    syndrome 9691
      Wiedemann Oldigs Oppermann Syndrome 0
Path 2
Term Annotations click to browse term
  disease 18145
    disease of anatomical entity 17519
      nervous system disease 13182
        central nervous system disease 11306
          brain disease 10593
            disease of mental health 7503
              developmental disorder of mental health 4869
                specific developmental disorder 4129
                  intellectual disability 3945
                    Wiedemann Oldigs Oppermann Syndrome 0
paths to the root