Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6812
Gene Symbol: STXBP1
STXBP1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 8289
Gene Symbol: ARID1A
ARID1A
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 3708
Gene Symbol: ITPR1
ITPR1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 55869
Gene Symbol: HDAC8
HDAC8
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 80152
Gene Symbol: CENPT
CENPT
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 23332
Gene Symbol: CLASP1
CLASP1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 22907
Gene Symbol: DHX30
DHX30
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 492
Gene Symbol: ATP2B3
ATP2B3
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 23126
Gene Symbol: POGZ
POGZ
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 51119
Gene Symbol: SBDS
SBDS
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 6595
Gene Symbol: SMARCA2
SMARCA2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 8785
Gene Symbol: MATN4
MATN4
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 285175
Gene Symbol: UNC80
UNC80
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 23141
Gene Symbol: ANKLE2
ANKLE2
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 767
Gene Symbol: CA8
CA8
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 51119
Gene Symbol: SBDS
SBDS
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 2022
Gene Symbol: ENG
ENG
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 9179
Gene Symbol: AP4M1
AP4M1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 2033
Gene Symbol: EP300
EP300
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 56131
Gene Symbol: PCDHB4
PCDHB4
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 79583
Gene Symbol: TMEM231
TMEM231
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR

Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 GeneticVariation CLINVAR

Entrez Id: 79053
Gene Symbol: ALG8
ALG8
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation CLINVAR