Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10084
Gene Symbol: PQBP1
PQBP1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.410 Biomarker HPO

Entrez Id: 25885
Gene Symbol: POLR1A
POLR1A
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.400 Biomarker HPO

Entrez Id: 3664
Gene Symbol: IRF6
IRF6
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.120 Biomarker HPO

Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 2316
Gene Symbol: FLNA
FLNA
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 1302
Gene Symbol: COL11A2
COL11A2
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 6309
Gene Symbol: SC5D
SC5D
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 8481
Gene Symbol: OFD1
OFD1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 1280
Gene Symbol: COL2A1
COL2A1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 CausalMutation CLINVAR

Entrez Id: 3480
Gene Symbol: IGF1R
IGF1R
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 157680
Gene Symbol: VPS13B
VPS13B
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 29980
Gene Symbol: DONSON
DONSON
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 6899
Gene Symbol: TBX1
TBX1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 545
Gene Symbol: ATR
ATR
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 GeneticVariation CLINVAR

Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 GeneticVariation CLINVAR

Entrez Id: 545
Gene Symbol: ATR
ATR
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 1280
Gene Symbol: COL2A1
COL2A1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.110 Biomarker HPO

Entrez Id: 84294
Gene Symbol: UTP23
UTP23
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 GeneticVariation CLINVAR A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 - Review of the literature. 30125677

2019

Entrez Id: 5885
Gene Symbol: RAD21
RAD21
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 GeneticVariation CLINVAR A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 - Review of the literature. 30125677

2019

Entrez Id: 8621
Gene Symbol: CDK13
CDK13
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 GeneticVariation CLINVAR Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. 28807008

2017

Entrez Id: 2186
Gene Symbol: BPTF
BPTF
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 GeneticVariation CLINVAR Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features. 28942966

2017

Entrez Id: 25
Gene Symbol: ABL1
ABL1
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.100 CausalMutation CLINVAR Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations. 28288113

2017