RGD Annotation Report for Hennekam Lymphangiectasia-Lymphedema Syndrome 2Rat Genome Database

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9 Annotations Found.

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens) & RGD:11558103\|RGD:126729603\|RGD:126733064\|RGD:126740061\|RGD:126762732\|RGD:12832998\|RGD:12835252\|RGD:12842897\|RGD:12843054\|RGD:12843489\|RGD:12844305\|RGD:12846996\|RGD:12900722\|RGD:12906716\|RGD:13212563\|RGD:14738684\|RGD:150406472\|RGD:150545996\|RGD:151731275\|RGD:151763143\|RGD:151767830\|RGD:151881919\|RGD:155900848\|RGD:156232020\|RGD:156404445\|RGD:156446894\|RGD:34890780 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from OMIM Disease Annotation Pipeline
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:8573704 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:22473091 PMID:24056717 PMID:24913602 PMID:2624276

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12848943 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:25741868 PMID:26325558 PMID:28492532

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens) & RGD:126729608\|RGD:126729612\|RGD:126740034\|RGD:126740048\|RGD:126740052\|RGD:126740056\|RGD:14739472\|RGD:150441745\|RGD:150451999\|RGD:155266611\|RGD:243051500\|RGD:38462753\|RGD:38463481\|RGD:405867675\|RGD:405867685\|RGD:405867687\|RGD:405867690\|RGD:405867693\|RGD:405867739 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:25741868

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:9589521 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:24913602 PMID:28492532

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:153348948 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:9589520\|RGD:9589522 (Homo sapiens) & RGD:9589520\|RGD:9589522 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:24913602

An association has been curated linking FAT4 and Hennekam Lymphangiectasia-Lymphedema Syndrome 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens) & RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens) & RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens) & RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens) & RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens) & RGD:12832962\|RGD:12838892\|RGD:12841977\|RGD:12845131\|RGD:12847271\|RGD:12847450 (Homo sapiens)
1 RGD objects have been annotated to Hennekam Lymphangiectasia-Lymphedema Syndrome 2 (DOID:9001947)
4 papers in RGD have been used to annotate FAT4
Curation Notes: ClinVar Annotator: match by term: Hennekam lymphangiectasia-lymphedema syndrome 2
Original References(s): PMID:24033266 PMID:25741868 PMID:28492532

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GENE - TERM ANNOTATION REPORT

9 Annotations Found.