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Term:cataract 36
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Accession:DOID:0110247 term browser browse the term
Definition:A cataract that has_material_basis_in homozygous mutation in the TDRD7 gene on chromosome 9q22.33. (DO)
Synonyms:exact_synonym: CATC4;   CTRCT36;   autosomal recessive congenital cataract 4
 primary_id: OMIM:613887
 alt_id: RDO:9000216
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cataract 36 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tdrd7 tudor domain containing 7 JBrowse link 5 61,557,909 61,631,719 RGD:7240710

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Term Annotations click to browse term
  disease 15992
    Developmental Diseases 9280
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8094
        genetic disease 7612
          cataract 36 1
Path 2
Term Annotations click to browse term
  disease 15992
    disease of anatomical entity 15263
      nervous system disease 10756
        sensory system disease 4969
          eye disease 2385
            lens disease 196
              cataract 189
                cataract 36 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.