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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:Unilateral Deafness with Delayed Endolymphatic Hydrops
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Accession:DOID:9001197 term browser browse the term
Synonyms:primary_id: MESH:C567420
 alt_id: MIM:612097


show annotations for term's descendants           Sort by:
Unilateral Deafness with Delayed Endolymphatic Hydrops term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Phex phosphate regulating endopeptidase X-linked ISO DNA:mutation:cds: RGD PMID:18289812 RGD:11556245 NCBI chr  X:37,607,553...37,856,183
Ensembl chr  X:37,610,760...37,854,469 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19106
    sensory system disease 7336
      Hearing Disorders 842
        Hearing Loss 837
          Unilateral Hearing Loss 4
            Unilateral Deafness with Delayed Endolymphatic Hydrops 1
Path 2
Term Annotations click to browse term
  disease 19106
    Pathological Conditions, Signs and Symptoms 13615
      Signs and Symptoms 11199
        Neurologic Manifestations 10433
          sensory system disease 7336
            Otorhinolaryngologic Diseases 1795
              auditory system disease 1055
                Hearing Disorders 842
                  Hearing Loss 837
                    Unilateral Hearing Loss 4
                      Unilateral Deafness with Delayed Endolymphatic Hydrops 1
paths to the root