Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3481
Gene Symbol: IGF2
IGF2
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.300 Biomarker CTD_human The consequent overexpression of Igf2 results in most of the symptoms of Beckwith-Wiedemann syndrome, including prenatal overgrowth, polyhydramnios, fetal and neonatal lethality, disproportionate organ overgrowth including tongue enlargement, and skeletal abnormalities. 9349812

1997

Entrez Id: 8216
Gene Symbol: LZTR1
LZTR1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 CausalMutation CLINVAR Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. 29469822

2018

Entrez Id: 8506
Gene Symbol: CNTNAP1
CNTNAP1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 GeneticVariation CLINVAR Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. 27668699

2017

Entrez Id: 8621
Gene Symbol: CDK13
CDK13
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
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: 673
Gene Symbol: BRAF
BRAF
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 GeneticVariation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008

Entrez Id: 5894
Gene Symbol: RAF1
RAF1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 CausalMutation CLINVAR Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. 17603483

2007

Entrez Id: 5894
Gene Symbol: RAF1
RAF1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 CausalMutation CLINVAR Germline gain-of-function mutations in RAF1 cause Noonan syndrome. 17603482

2007

Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 57190
Gene Symbol: SELENON
SELENON
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 219844
Gene Symbol: HYLS1
HYLS1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 6261
Gene Symbol: RYR1
RYR1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 9935
Gene Symbol: MAFB
MAFB
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 3295
Gene Symbol: HSD17B4
HSD17B4
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 72
Gene Symbol: ACTG2
ACTG2
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 7170
Gene Symbol: TPM3
TPM3
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 10916
Gene Symbol: MAGED2
MAGED2
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 342035
Gene Symbol: GLDN
GLDN
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 57465
Gene Symbol: TBC1D24
TBC1D24
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 6576
Gene Symbol: SLC25A1
SLC25A1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 1785
Gene Symbol: DNM2
DNM2
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 23169
Gene Symbol: SLC35D1
SLC35D1
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 55975
Gene Symbol: KLHL7
KLHL7
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 4703
Gene Symbol: NEB
NEB
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO

Entrez Id: 9508
Gene Symbol: ADAMTS3
ADAMTS3
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0.100 Biomarker HPO