Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
0.700 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.700 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.700 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.500 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.430 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0152423
Disease: Congenital small ears
Congenital small ears
0.410 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C1833340
Disease: Synostotic Posterior Plagiocephaly
Synostotic Posterior Plagiocephaly
0.410 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.410 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0030044
Disease: Acrocephaly
Acrocephaly
0.400 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
0.400 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly
0.400 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius
0.400 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.160 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
0.120 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0265886
Disease: Overriding aorta
Overriding aorta
0.110 Biomarker HPO

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis
0.110 Biomarker HPO