Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | FGFR2 | Human | 2-Methylbutyryl-CoA Dehydrogenase Deficiency | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Deficiency of 2-methylbutyryl-CoA dehydrogenase | ClinVar | PMID:20547083 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:16418739 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:24728327 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:11781872 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:24728327 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:28492532 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:25741868 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:24127277 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:11173845 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:12884424 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:17576681 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:25741868 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial-skeletal-dermatologic dysplasia | ClinVar | PMID:12400058 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:12000365 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:10951518 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:24728327 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:11781872 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:10851026 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:16158432 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:11870239 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:10618369 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:11390973 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:10851026 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:17264867 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:11781872 more ... | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephaly more ... | ClinVar | PMID:26467025 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:9973282 | FGFR2 | Human | acrocephalosyndactylia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly type I | ClinVar | PMID:10394936 more ... | FGFR2 | Human | adenoid cystic carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Adenoid cystic carcinoma | ClinVar | PMID:26619011 | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:10076886 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Antley-Bixler syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:10076886 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Antley-Bixler syndrome with disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Osteodysgenesis and multisynostotic with fractures | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:25741868 | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:10076886 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:10633130 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:10541159 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Antley-Bixler syndrome without disordered steroidogenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Beare-Stevenson cutis gyrata syndrome | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:28492532 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:18247426 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Beare-Stevenson cutis gyrata syndrome | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Beare-Stevenson cutis gyrata syndrome | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:17264867 more ... | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cutis Gyrata syndrome of Beare and Stevenson | ClinVar | PMID:26467025 | FGFR2 | Human | Beare-Stevenson cutis gyrata syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Beare-Stevenson cutis gyrata syndrome | ClinVar | PMID:19610084 | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:12000365 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:25741868 | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:11390973 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:25741868 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:24728327 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bent bone dysplasia syndrome 1 | ClinVar | PMID:11781872 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related bent bone dysplasia | ClinVar | PMID:22387015 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:16158432 more ... | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bent bone dysplasia syndrome 1 | ClinVar | PMID:22387015 | FGFR2 | Human | bent bone dysplasia syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: BENT BONE DYSPLASIA SYNDROME 1 | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Breast Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Breast Neoplasms | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | Breast Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Breast Neoplasms | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | Breast Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Breast neoplasm | ClinVar | PMID:18552176 more ... | FGFR2 | Human | Breast Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Breast Neoplasms | ClinVar | PMID:17525745 and PMID:26619011 | FGFR2 | Human | colorectal cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Colorectal cancer | ClinVar | | FGFR2 | Human | Congenital Aural Atresia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: AURAL ATRESIA more ... | ClinVar | PMID:23786770 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:25174698 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10574673 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:22117175 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:24728327 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:24728327 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:21928350 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:17576681 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12575301 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:28492532 and PMID:8644708 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:25741868 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:17803937 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:21524234 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12884424 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:24728327 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11390973 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10076886 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11556600 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:24127277 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11556600 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:25741868 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10874645 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12884424 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:17576681 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11173845 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:27028366 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:18391498 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16199547 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:25741868 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:28492532 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16501574 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:18247426 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:25271085 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11173845 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12400058 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:28492532 and PMID:31754721 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:27527345 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:21524234 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:18618990 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12884424 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:12000365 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:17873121 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10874645 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10067911 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10951518 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11173845 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10633130 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:26467025 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:23995961 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:15523615 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:28492532 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10851026 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:16158432 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:25640679 and PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11870239 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10618369 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10541159 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10851026 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11390973 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:11781872 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:17264867 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis 1 | ClinVar | PMID:26467025 | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:16418739 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:10394936 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis | ClinVar | PMID:24728327 more ... | FGFR2 | Human | craniosynostosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FGFR2-related craniosynostosis | ClinVar | PMID:17803937 and PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:17803937 and PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:25741868 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:15523615 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:17264867 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:26467025 | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Craniosynostosis Syndrome, Autosomal Recessive | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | PMID:17803937 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis type 1 | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:28492532 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:12884424 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis type 1 | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis | ClinVar | PMID:10076886 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11556600 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis type 1 | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:27028366 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis type 1 | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:25271085 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10874645 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10067911 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10951518 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10633130 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:23995961 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniofacial dysostosis type 1 | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11870239 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:16061565 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10541159 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:17264867 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:26467025 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:16061565 and PMID:9169049 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:8528214 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon disease | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | Crouzon syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Crouzon syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | disorder of sexual development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Disorder of sexual differentiation | ClinVar | | FGFR2 | Human | endometrial carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial carcinoma | ClinVar | PMID:10851026 more ... | FGFR2 | Human | endometrial carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial carcinoma | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:17525745 | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:18247426 more ... | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:25157968 | FGFR2 | Human | Endometrial Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial neoplasm | ClinVar | PMID:17525745 and PMID:26619011 | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:23908597 | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:18552176 more ... | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | Endometrioid Carcinomas | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Endometrial Endometrioid Adenocarcinoma and Variant with Squamous Differentiation | ClinVar | PMID:18552176 more ... | FGFR2 | Human | esophageal carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Esophageal carcinoma | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | esophageal carcinoma | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Carcinoma of esophagus | ClinVar | PMID:26619011 | FGFR2 | Human | gastric adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastric adenocarcinoma | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | gastric adenocarcinoma | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastric adenocarcinoma | ClinVar | PMID:26619011 | FGFR2 | Human | gastric adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastric adenocarcinoma | ClinVar | PMID:10851026 more ... | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:10618369 more ... | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:10067911 more ... | FGFR2 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:22387015 more ... | FGFR2 | Human | head and neck cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Head and neck neoplasm | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Head and Neck Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Head and Neck Neoplasms | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Hypertelorism | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertelorism | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:12884424 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:11556600 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:12884424 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:10633130 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis more ... | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Jackson-Weiss syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jackson-Weiss syndrome | ClinVar | PMID:10541159 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:12000365 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:11390973 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:25741868 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:25741868 | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 and PMID:18056630 | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16158432 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 | FGFR2 | Human | lacrimoauriculodentodigital syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 and PMID:18056630 | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:12000365 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:11390973 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:25741868 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: LADD syndrome | ClinVar | PMID:16158432 more ... | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | | FGFR2 | Human | LADD syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Levy-Hollister syndrome | ClinVar | PMID:16501574 | FGFR2 | Human | lung adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lung adenocarcinoma | ClinVar | PMID:17525745 and PMID:26619011 | FGFR2 | Human | lung adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lung adenocarcinoma | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | lung adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Adenocarcinoma of lung | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | lung adenocarcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lung adenocarcinoma | ClinVar | PMID:18552176 more ... | FGFR2 | Human | lung squamous cell carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Squamous cell lung carcinoma | ClinVar | PMID:23786770 | FGFR2 | Human | lung squamous cell carcinoma | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Squamous cell lung carcinoma | ClinVar | | FGFR2 | Human | lung squamous cell carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Squamous cell lung carcinoma | ClinVar | PMID:23786770 more ... | FGFR2 | Human | Nasopharyngeal Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nasopharyngeal neoplasm | ClinVar | PMID:17525745 and PMID:26619011 | FGFR2 | Human | Nasopharyngeal Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nasopharyngeal neoplasm | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | Nasopharyngeal Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nasopharyngeal Neoplasms | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | Nasopharyngeal Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nasopharyngeal neoplasm | ClinVar | PMID:18552176 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:12884424 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:10076886 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:11556600 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:12400058 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10874645 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10633130 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:15523615 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:23786770 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acrocephalosyndactyly and type 5 | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10541159 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:16061565 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:16418739 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:11781872 and PMID:23348274 | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10394936 | FGFR2 | Human | Pfeiffer syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pfeiffer syndrome | ClinVar | PMID:10945669 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chotzen syndrome | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:25741868 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:28492532 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:24728327 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chotzen syndrome | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:26325558 and PMID:28492532 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chotzen syndrome | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chotzen syndrome | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar more ... | ClinVar | | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:24728327 and PMID:28492532 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:17264867 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:11781872 more ... | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chotzen syndrome | ClinVar | PMID:26467025 | FGFR2 | Human | Saethre-Chotzen syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Saethre-Chotzen syndrome | ClinVar | PMID:9585583 | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:25741868 | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:25741868 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:16061565 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Scaphocephaly, Maxillary Retrusion, and Impaired Intellectual Development | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SCAPHOCEPHALY more ... | ClinVar | PMID:24728327 more ... | FGFR2 | Human | sensorineural hearing loss | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bilateral sensorineural hearing impairment | ClinVar | PMID:19461658 more ... | FGFR2 | Human | split hand-foot malformation | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ectrodactyly | ClinVar | PMID:25741868 | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Stomach cancer | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach cancer | ClinVar | PMID:25741868 more ... | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastric cancer | ClinVar | PMID:10394936 more ... | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach cancer | ClinVar | PMID:16158432 more ... | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach cancer | ClinVar | PMID:24728327 more ... | FGFR2 | Human | stomach cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach cancer | ClinVar | PMID:10851026 more ... | FGFR2 | Human | Stomach Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach Neoplasms | ClinVar | PMID:12000365 more ... | FGFR2 | Human | Stomach Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach Neoplasms | ClinVar | PMID:11390973 more ... | FGFR2 | Human | Stomach Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastric neoplasm | ClinVar | PMID:16158432 more ... | FGFR2 | Human | Stomach Neoplasms | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Stomach Neoplasms | ClinVar | PMID:25741868 and PMID:28492532 | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:17525745 and PMID:26619011 | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:25157968 and PMID:26619011 | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:26619011 | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:10851026 more ... | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:18552176 more ... | FGFR2 | Human | uterine cancer | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Malignant neoplasm of body of uterus | ClinVar | PMID:23908597 and PMID:26619011 | FGFR2 | Human | uterine carcinosarcoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Uterine carcinosarcoma | ClinVar | PMID:10851026 more ... | |
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Imported Disease Annotations - CTD
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