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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking CDON and holoprosencephaly 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:151710784 (Homo sapiens)
  • 239 RGD objects have been annotated to holoprosencephaly  (DOID:4621)
  • 10 papers in RGD have been used to annotate CDON
  • Curation Notes: ClinVar Annotator: match by term: Holoprosencephaly spectrum disorder
  • Original References(s): PMID:20301702 PMID:26728615 PMID:28492532


    • An association has been curated linking CDON and holoprosencephaly 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:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens) & RGD:11606387|RGD:11610379|RGD:11613514|RGD:11614367|RGD:11634943|RGD:11635176|RGD:11635457|RGD:11635472|RGD:11635867|RGD:11646490|RGD:11653412|RGD:11653855|RGD:11655532|RGD:11657180|RGD:11659970|RGD:11661501|RGD:11662350|RGD:11662714|RGD:11665647|RGD:11666822 (Homo sapiens)
  • 239 RGD objects have been annotated to holoprosencephaly  (DOID:4621)
  • 10 papers in RGD have been used to annotate CDON
  • Curation Notes: ClinVar Annotator: match by term: Holoprosencephaly sequence


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