FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 731; N. variants: 141
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1867564
Disease: SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY 		0.400 CausalMutation disease CLINVAR
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.360 CausalMutation disease CGI
CUI: C1153706
Disease: Endometrial adenocarcinoma
Endometrial adenocarcinoma 		0.320 CausalMutation disease CGI
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.310 Biomarker disease GENOMICS_ENGLAND
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		0.300 CausalMutation disease CGI
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		0.300 GenomicAlterations disease CGI
CUI: C0154060
Disease: Carcinoma in situ of stomach
Carcinoma in situ of stomach 		0.300 GenomicAlterations disease CGI
CUI: C0154060
Disease: Carcinoma in situ of stomach
Carcinoma in situ of stomach 		0.300 CausalMutation disease CGI
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		0.300 CausalMutation disease CGI
CUI: C0346191
Disease: Carcinoma in situ of endometrium
Carcinoma in situ of endometrium 		0.300 CausalMutation disease CGI
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		0.300 CausalMutation disease CGI
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		0.300 GenomicAlterations disease CGI
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly 		0.300 Biomarker disease CTD_human
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma 		0.300 CausalMutation disease CGI
CUI: C0021828
Disease: Intestinal Atresia
Intestinal Atresia 		0.200 Biomarker disease MGD
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.160 Biomarker disease HPO
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.120 Biomarker disease HPO
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.120 CausalMutation disease CLINVAR
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		0.110 Biomarker disease HPO
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		0.110 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.110 Biomarker disease HPO
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		0.110 Biomarker disease HPO
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.110 Biomarker group HPO
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.110 Biomarker group HPO