Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

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:Usher syndrome type 2D
go back to main search page
Accession:DOID:0110840 term browser browse the term
Definition:An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32. (DO)
Synonyms:exact_synonym: USH2D;   Usher Syndrome, Type IID
 primary_id: OMIM:611383;   RDO:0009522
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
Usher syndrome type 2D term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Whrn whirlin ISO
IEA
ClinVar Annotator: match by OMIM:611383
ClinVar Annotator: match by term: Usher syndrome, type 2D
OMIM
ClinVar
MouseDO
PMID:15841483 PMID:17171570 PMID:20352026 PMID:21569298 PMID:21654738 PMID:22135276 PMID:22147658 PMID:23804846 PMID:24033266 PMID:25262649 PMID:25404053 PMID:25468891 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30245029 NCBI chr 4:63,414,908...63,496,083
Ensembl chr 4:63,414,910...63,495,991
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13447
    syndrome 6558
      Usher syndrome 52
        Usher syndrome type 2 13
          Usher syndrome type 2D 1
Path 2
Term Annotations click to browse term
  disease 13447
    disease of anatomical entity 12920
      nervous system disease 10471
        sensory system disease 5060
          Otorhinolaryngologic Diseases 1199
            auditory system disease 760
              Hearing Disorders 614
                Hearing Loss 609
                  Deafness 282
                    Deaf-Blind Disorders 60
                      Usher syndrome 52
                        Usher syndrome type 2 13
                          Usher syndrome type 2D 1
paths to the root