GDF3, growth differentiation factor 3, 9573

N. diseases: 74; N. variants: 4
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		0.600 Biomarker disease GENOMICS_ENGLAND Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies. 19864492 2010
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		0.600 Biomarker disease GENOMICS_ENGLAND Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies. 19864492 2010
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		0.600 GeneticVariation disease UNIPROT Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies. 19864492 2010
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		0.600 Biomarker disease CTD_human
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		0.600 Biomarker disease GENOMICS_ENGLAND