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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:cataract 43
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Accession:DOID:0110259 term browser browse the term
Definition:A cataract that has_material_basis_in heterozygous mutation in the UNC45B gene on chromosome 17q12. (DO)
Synonyms:exact_synonym: CTRCT43
 primary_id: OMIM:616279

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cataract 43 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G UNC45B unc-45 myosin chaperone B ISO ClinVar Annotator: match by term: Cataract 43 OMIM
ClinVar		 PMID:24549050 PMID:25741868 NCBI chr16:28,649,541...28,690,467 JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15273
    sensory system disease 6524
      eye disease 3344
        lens disease 412
          cataract 402
            cataract 43 1
Path 2
Term Annotations click to browse term
  disease 15273
    Pathological Conditions, Signs and Symptoms 11780
      Signs and Symptoms 9744
        Neurologic Manifestations 9422
          sensory system disease 6524
            eye disease 3344
              lens disease 412
                cataract 402
                  cataract 43 1
paths to the root