Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:hereditary papulotranslucent acrokeratoderma
go back to main search page
Accession:DOID:0060360 term browser browse the term
Definition:A keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis. (DO)
Synonyms:primary_id: MESH:C566323
 alt_id: OMIM:101840;   RDO:0014709
For additional species annotation, visit the Alliance of Genome Resources.



show annotations for term's descendants           Sort by:
 

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 20286
    sensory system disease 6214
      skin disease 3153
        keratosis 163
          hereditary papulotranslucent acrokeratoderma 0
Path 2
Term Annotations click to browse term
  disease 20286
    disease of anatomical entity 18890
      nervous system disease 14866
        sensory system disease 6214
          skin disease 3153
            keratosis 163
              cholesteatoma 21
                hereditary papulotranslucent acrokeratoderma 0
paths to the root