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1 Annotations Found.

An association has been curated linking BCAP31 and Contiguous Abcd1/Dxs1375e Deletion Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 CRRD objects have been annotated to Contiguous Abcd1/Dxs1375e Deletion Syndrome  (DOID:9005157)
  • 7 papers in CRRD have been used to annotate BCAP31

  • This annotation was curated on 2019-09-11 19:57:08.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.