Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 GeneticVariation disease CLINVAR A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort. 24065355 2013
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 GeneticVariation disease BEFREE A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort. 24065355 2013
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 CausalMutation disease CLINVAR A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort. 24065355 2013
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 GermlineCausalMutation disease ORPHANET A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort. 24065355 2013
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 CausalMutation disease CLINVAR Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. 17160902 2007
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
0.610 Biomarker disease CTD_human