Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56776
Gene Symbol: FMN2
FMN2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 1968
Gene Symbol: EIF2S3
EIF2S3
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 171023
Gene Symbol: ASXL1
ASXL1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 50485
Gene Symbol: SMARCAL1
SMARCAL1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 9373
Gene Symbol: PLAA
PLAA
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 57479
Gene Symbol: PRR12
PRR12
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 84947
Gene Symbol: SERAC1
SERAC1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 9927
Gene Symbol: MFN2
MFN2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 7274
Gene Symbol: TTPA
TTPA
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 5190
Gene Symbol: PEX6
PEX6
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 79813
Gene Symbol: EHMT1
EHMT1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 118426
Gene Symbol: BORCS5
BORCS5
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 11113
Gene Symbol: CIT
CIT
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 11128
Gene Symbol: POLR3A
POLR3A
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 9757
Gene Symbol: KMT2B
KMT2B
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 9343
Gene Symbol: EFTUD2
EFTUD2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 57038
Gene Symbol: RARS2
RARS2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 79644
Gene Symbol: SRD5A3
SRD5A3
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 81857
Gene Symbol: MED25
MED25
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 57728
Gene Symbol: WDR19
WDR19
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 51010
Gene Symbol: EXOSC3
EXOSC3
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 5859
Gene Symbol: QARS1
QARS1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 2132
Gene Symbol: EXT2
EXT2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 10084
Gene Symbol: PQBP1
PQBP1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 79876
Gene Symbol: UBA5
UBA5
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR