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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:Rud Syndrome
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Accession:DOID:9006451 term browser browse the term
Synonyms:exact_synonym: Dwarfism ichthyosiform erythroderma mental deficiency syndrome;   Ichthyosis hypogonadism mental retardation epilepsy syndrome;   Ichthyosis male hypogonadism syndrome;   Ichthyosis oligophrenia epilepsy syndrome;   Neuroichthyosis hypogonadism syndrome;   Rud's syndrome
 primary_id: MESH:C535878
 alt_id: RDO:0001231
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 17129
    syndrome 8018
      Rud Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17129
    disease of anatomical entity 16476
      nervous system disease 12074
        central nervous system disease 10353
          brain disease 9712
            disease of mental health 7022
              developmental disorder of mental health 4362
                specific developmental disorder 3621
                  intellectual disability 3433
                    Rud Syndrome 0
paths to the root