Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Axenfeld-Rieger syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Rieger anomaly | ClinVar | PMID:26893459 and PMID:28492532 | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract | ClinVar | PMID:28844315 and PMID:34246755 | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | PMID:12766769 more ... | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | PMID:30143558 | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | PMID:30143558 | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | PMID:25741868 | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | | CAKUT | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar | PMID:25741868 | congenital diaphragmatic hernia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital diaphragmatic hernia | ClinVar | | congenital diaphragmatic hernia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Agenesis of hemidiaphragm | ClinVar | PMID:25741868 | congenital diaphragmatic hernia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital diaphragmatic hernia | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos with other malformations | ClinVar | PMID:12766769 more ... | Fraser syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos with other malformations | ClinVar | PMID:28844315 and PMID:34246755 | Fraser syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos with other malformations | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:18671281 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:17576681 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:17576681 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:17576681 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:17576681 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24700879 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24476948 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24700879 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:35005812 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:35005812 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:35005812 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24476948 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRAS1-related condition | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28844315 and PMID:34246755 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:34974531 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:18671281 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:18671281 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:18671281 and PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24551978 and PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:12766769 and PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:21900877 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:25741868 and PMID:31319225 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:24583203 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:23532946 more ... | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cryptophthalmos syndrome | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:16894541 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:27280866 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:17163535 and PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:12766769 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:12766769 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:12766769 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:12766769 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:25741868 and PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fraser syndrome 1 | ClinVar | PMID:28492532 | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | Fraser syndrome 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FRASER SYNDROME 1 | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:32643034 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | microcephaly | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Microcephaly | ClinVar | PMID:25741868 and PMID:28492532 | myoepithelioma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Myoepithelial tumor | ClinVar | | renal agenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Renal agenesis | ClinVar | PMID:25741868 and PMID:35005812 | renal agenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Renal agenesis | ClinVar | PMID:25741868 and PMID:35005812 | renal agenesis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Renal agenesis | ClinVar | PMID:25741868 and PMID:35005812 | syndromic microphthalmia 5 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Anophthalmia-microphthalmia syndrome | ClinVar | PMID:24700879 more ... | Usher syndrome type 2C | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Usher syndrome and type 2C | ClinVar | PMID:21900877 more ... | |