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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 8
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Accession:DOID:0110527 term browser browse the term
Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22. (DO)
Synonyms:exact_synonym: DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8;   DFNB10;   DFNB8;   Deafness, Autosomal Recessive 10;   Deafness, Autosomal Recessive 8/10;   NRSD8;   NSRD8;   Neurosensory Nonsyndromic Recessive Deafness 8;   TMPRSS3-RELATED CONDITION;   autosomal recessive deafness 8
 primary_id: MESH:C563395;   MESH:C565341;   OMIM:601072;   RDO:0012661
 alt_id: RDO:0008796;   RDO:0014006


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16465
    sensory system disease 6279
      Hearing Disorders 732
        Hearing Loss 727
          sensorineural hearing loss 548
            autosomal recessive nonsyndromic deafness 135
              autosomal recessive nonsyndromic deafness 8 1
Path 2
Term Annotations click to browse term
  disease 16465
    Pathological Conditions, Signs and Symptoms 11287
      Signs and Symptoms 9356
        Neurologic Manifestations 9046
          sensory system disease 6279
            Otorhinolaryngologic Diseases 1589
              auditory system disease 897
                Hearing Disorders 732
                  Hearing Loss 727
                    Deafness 355
                      nonsyndromic deafness 207
                        autosomal recessive nonsyndromic deafness 135
                          autosomal recessive nonsyndromic deafness 8 1
paths to the root