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ONTOLOGY REPORT - ANNOTATIONS


Term:cataract 39 multiple types
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Accession:DOID:0110236 term browser browse the term
Definition:A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34. (DO)
Synonyms:exact_synonym: CTRCT39;   autosomal dominant cataract 39 multiple types;   autosomal dominant cataract, multiple types 2
 primary_id: OMIM:615188
 alt_id: RDO:9000218
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cataract 39 multiple types term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Crygb crystallin, gamma B JBrowse link 9 71,796,204 71,798,265 RGD:7240710
RGD:8554872

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Term Annotations click to browse term
  disease 15639
    Developmental Diseases 8774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7556
        genetic disease 7052
          monogenic disease 4684
            cataract 188
              cataract 39 multiple types 1
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      nervous system disease 10242
        sensory system disease 4697
          eye and adnexa disease 2257
            eye disease 2257
              lens disease 195
                cataract 188
                  cataract 39 multiple types 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.