Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0009806
Disease: Constipation
Constipation 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0042798
Disease: Low Vision
Low Vision 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C4024166
Disease: Crumpled ear
Crumpled ear 		0.100 GeneticVariation CLINVAR

Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C4317146
Disease: Acid reflux
Acid reflux 		0.100 GeneticVariation CLINVAR