ORC4, origin recognition complex subunit 4, 5000

N. diseases: 75; N. variants: 28
Disease: MEIER-GORLIN SYNDROME 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 Biomarker disease GENOMICS_ENGLAND Meier-Gorlin syndrome. 26381604 2015
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in the pre-replication complex cause Meier-Gorlin syndrome. 21358632 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 CausalMutation disease CLINVAR Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. 21358631 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in the pre-replication complex cause Meier-Gorlin syndrome. 21358632 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 GeneticVariation disease UNIPROT Mutations in the pre-replication complex cause Meier-Gorlin syndrome. 21358632 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 GeneticVariation disease UNIPROT Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. 21358631 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 CausalMutation disease CLINVAR Mutations in the pre-replication complex cause Meier-Gorlin syndrome. 21358632 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 GeneticVariation disease CLINVAR Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. 21358631 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 GeneticVariation disease CLINVAR Mutations in the pre-replication complex cause Meier-Gorlin syndrome. 21358632 2011
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 Biomarker disease GENOMICS_ENGLAND Meier-Gorlin syndrome: report of eight additional cases and review. 11477602 2001
CUI: C3151097
Disease: MEIER-GORLIN SYNDROME 2
MEIER-GORLIN SYNDROME 2 		0.600 Biomarker disease GENOMICS_ENGLAND Assignment of the homologue of the yeast origin recognition complex subunit ORC4 (ORC4L) to human chromosome band 2q22-->q23 by in situ hybridization and somatic cell hybrid analysis. 9691185 1998