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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV264778 and hypomyelinating leukodystrophy 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 3 RGD objects have been annotated to hypomyelinating leukodystrophy 2  (DOID:0060787)
  • 0 papers in RGD have been used to annotate CV264778
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelinating leukodystrophy 2
  • Original References(s): PMID:15968592 PMID:21073448 PMID:25356970 PMID:25741868 PMID:28492532 PMID:31748968 PMID:33977139


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