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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking ABHD16A and hereditary spastic paraplegia 86 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 86  (DOID:0112342)
  • 2 papers in RGD have been used to annotate ABHD16A


    • An association has been curated linking ABHD16A and hereditary spastic paraplegia 86 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:151661153 (Homo sapiens)
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 86  (DOID:0112342)
  • 2 papers in RGD have been used to annotate ABHD16A
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 86, autosomal recessive
  • Original References(s): PMID:34866177


    • An association has been curated linking ABHD16A and hereditary spastic paraplegia 86 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:401946468 (Homo sapiens)
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 86  (DOID:0112342)
  • 2 papers in RGD have been used to annotate ABHD16A
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 86, autosomal recessive
  • Original References(s): PMID:25741868


    • An association has been curated linking ABHD16A and hereditary spastic paraplegia 86 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:150508194|RGD:150508198|RGD:150508204 (Homo sapiens) & RGD:150508194|RGD:150508198|RGD:150508204 (Homo sapiens) & RGD:150508194|RGD:150508198|RGD:150508204 (Homo sapiens)
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 86  (DOID:0112342)
  • 2 papers in RGD have been used to annotate ABHD16A
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 86, autosomal recessive
  • Original References(s): PMID:25741868 PMID:34587489


    • An association has been curated linking ABHD16A and hereditary spastic paraplegia 86 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:150416313|RGD:150416314 (Homo sapiens) & RGD:150416313|RGD:150416314 (Homo sapiens)
  • 1 RGD objects have been annotated to hereditary spastic paraplegia 86  (DOID:0112342)
  • 2 papers in RGD have been used to annotate ABHD16A
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 86, autosomal recessive


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