Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Child Development Disorders, Pervasive
0.100 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma
0.100 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0677865
Disease: Brain Stem Glioma
Brain Stem Glioma
0.100 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Acute lymphoblastic leukemia with lymphomatous features
0.100 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.100 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0002170
Disease: Alopecia
Alopecia
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003126
Disease: Anosmia
Anosmia
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003467
Disease: Anxiety
Anxiety
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003537
Disease: Aphasia
Aphasia
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0004096
Disease: Asthma
Asthma
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0005937
Disease: Bone Cysts
Bone Cysts
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0009398
Disease: Color vision defect
Color vision defect
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0009806
Disease: Constipation
Constipation
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome
0.100 Biomarker HPO

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0011848
Disease: Diabetes Insipidus
Diabetes Insipidus
0.100 Biomarker HPO