FGFR3, fibroblast growth factor receptor 3, 2261

N. diseases: 654; N. variants: 55
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.600 CausalMutation disease CGI
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.540 Biomarker disease CTD_human
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.510 Biomarker disease CTD_human
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.510 CausalMutation disease CGI
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		0.500 CausalMutation disease CLINVAR
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.500 CausalMutation disease CGI
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.500 CausalMutation disease CGI
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.500 GeneticVariation disease UNIPROT
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		0.500 Biomarker disease CTD_human
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.460 CausalMutation disease CLINVAR
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.460 CausalMutation disease CGI
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		0.420 Biomarker disease HPO
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		0.410 CausalMutation disease CLINVAR
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		0.410 GeneticVariation disease ORPHANET
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.410 Biomarker disease HPO
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 Biomarker phenotype HPO
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 GeneticVariation phenotype CLINVAR
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.400 Biomarker disease HPO
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.400 Biomarker disease HPO
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		0.400 Biomarker disease GENOMICS_ENGLAND
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		0.400 Biomarker disease HPO
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.340 CausalMutation disease CGI
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.300 Biomarker group CTD_human
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.300 Biomarker disease MGD