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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:Autosomal Recessive Nonsyndromic Deafness 118
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Accession:DOID:9004101 term browser browse the term
Synonyms:exact_synonym: DFNB118;   autosomal recessive deafness 118, with cochlear aplasia
 primary_id: OMIM:619553


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17773
    sensory system disease 6589
      Hearing Disorders 774
        Hearing Loss 769
          sensorineural hearing loss 584
            autosomal recessive nonsyndromic deafness 139
              Autosomal Recessive Nonsyndromic Deafness 118 0
Path 2
Term Annotations click to browse term
  disease 17773
    Pathological Conditions, Signs and Symptoms 12020
      Signs and Symptoms 9897
        Neurologic Manifestations 9572
          sensory system disease 6589
            Otorhinolaryngologic Diseases 1674
              auditory system disease 950
                Hearing Disorders 774
                  Hearing Loss 769
                    Deafness 369
                      nonsyndromic deafness 215
                        autosomal recessive nonsyndromic deafness 139
                          Autosomal Recessive Nonsyndromic Deafness 118 0
paths to the root