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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking DCX and NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:153349494 (Homo sapiens)
  • 29 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  (DOID:9001150)
  • 23 papers in RGD have been used to annotate DCX
  • Curation Notes: ClinVar Annotator: match by term: Abnormality of the cerebrum


    • An association has been curated linking DCX and NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562590 (Homo sapiens)
  • 29 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  (DOID:9001150)
  • 23 papers in RGD have been used to annotate DCX
  • Curation Notes: ClinVar Annotator: match by term: Abnormality of the cerebrum
  • Original References(s): PMID:11175293 PMID:11468322 PMID:18414213 PMID:18685874 PMID:23365099 PMID:25741868 PMID:28492532 PMID:35213059


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