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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:facial dermatosis
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Accession:DOID:3134 term browser browse the term
Definition:Skin diseases involving the FACE.
Synonyms:exact_synonym: Favre Racouchot Syndrome;   Nodular Elastoidoses;   Nodular Elastoidosis;   Nodular Elastoses;   Nodular Elastosis;   facial dermatoses
 primary_id: MESH:D005148
 xref: EFO:1000698
For additional species annotation, visit the Alliance of Genome Resources.


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facial dermatosis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G C9 complement C9 ISO CTD Direct Evidence: marker/mechanism CTD PMID:11359403 NCBI chr 2:55,573,094...55,621,345
Ensembl chr 2:55,572,992...55,621,338 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    sensory system disease 6961
      skin disease 3968
        facial dermatosis 1
          Congenital Facial Linear Porokeratosis 0
          Judge Misch Wright Syndrome 0
          Perioral Dermatitis 0
          Rombo Syndrome 0
          Sebaceous Gland Hyperplasia, Familial Presenile 0
Path 2
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18249
      nervous system disease 14091
        Neurologic Manifestations 10055
          sensory system disease 6961
            skin disease 3968
              facial dermatosis 1
                Congenital Facial Linear Porokeratosis 0
                Judge Misch Wright Syndrome 0
                Perioral Dermatitis 0
                Rombo Syndrome 0
                Sebaceous Gland Hyperplasia, Familial Presenile 0
paths to the root