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Term:cataract 35
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Accession:DOID:0110261 term browser browse the term
Definition:A cataract that has_material_basis_in variation in the region 19q13. (DO)
Synonyms:exact_synonym: CATCN1;   CTRCT35;   autosomal recessive congenital nuclear cataract 1;   cataract 35, congenital nuclear
 primary_id: MESH:C563728;   RDO:0012913
 alt_id: OMIM:609376
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Path 1
Term Annotations click to browse term
  disease 15603
    Developmental Diseases 8772
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7555
        genetic disease 7051
          Hereditary Eye Diseases 505
            cataract 35 0
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      nervous system disease 10239
        sensory system disease 4697
          eye and adnexa disease 2259
            eye disease 2259
              lens disease 195
                cataract 188
                  cataract 35 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.