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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:Bifid Nose
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Accession:DOID:9003807 term browser browse the term
Synonyms:exact_synonym: Bifid Nose, Autosomal Dominant;   Bifid Nose, Autosomal Recessive;   Median fissure of nose;   median cleft of nose
 primary_id: MESH:C535441
 alt_id: OMIM:109740;   OMIM:210400
For additional species annotation, visit the Alliance of Genome Resources.


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Bifid Nose term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Frem1 Fras1 related extracellular matrix 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:23221805 NCBI chr 5:97,321,275...97,469,523
Ensembl chr 5:97,322,538...97,469,543 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 0
    sensory system disease 7072
      Otorhinolaryngologic Diseases 1819
        nose disease 230
          Bifid Nose 1
Path 2
Term Annotations click to browse term
  disease 20985
    disease of anatomical entity 18153
      nervous system disease 14091
        Neurologic Manifestations 0
          sensory system disease 7072
            Otorhinolaryngologic Diseases 1819
              nose disease 230
                Bifid Nose 1
paths to the root