Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51053
Gene Symbol: GMNN
GMNN 		0.100 CausalMutation phenotype CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
Entrez Id: 2074
Gene Symbol: ERCC6
ERCC6 		0.100 Biomarker phenotype HPO
Entrez Id: 57061
Gene Symbol: HYMAI
HYMAI 		0.100 Biomarker phenotype HPO
Entrez Id: 2817
Gene Symbol: GPC1
GPC1 		0.100 Biomarker phenotype HPO
Entrez Id: 9896
Gene Symbol: FIG4
FIG4 		0.100 Biomarker phenotype HPO
Entrez Id: 5190
Gene Symbol: PEX6
PEX6 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 25914
Gene Symbol: RTTN
RTTN 		0.100 Biomarker phenotype HPO
Entrez Id: 5230
Gene Symbol: PGK1
PGK1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 346171
Gene Symbol: ZFP57
ZFP57 		0.100 Biomarker phenotype HPO
Entrez Id: 538
Gene Symbol: ATP7A
ATP7A 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 5191
Gene Symbol: PEX7
PEX7 		0.100 Biomarker phenotype HPO
Entrez Id: 3643
Gene Symbol: INSR
INSR 		0.100 Biomarker phenotype HPO
Entrez Id: 55697
Gene Symbol: VAC14
VAC14 		0.100 Biomarker phenotype HPO
Entrez Id: 5631
Gene Symbol: PRPS1
PRPS1 		0.100 Biomarker phenotype HPO