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| Hereditary Haemorrhagic Telangiectasia v2.0 | DROSHA | Gene migrated from ENSG00000113360 to ENSG00000113360 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Haemorrhagic Telangiectasia v1.6 | Bryony Thompson Copied gene DROSHA from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Haemorrhagic Telangiectasia v1.6 | DROSHA |
Bryony Thompson gene: DROSHA was added gene: DROSHA was added to Hereditary Haemorrhagic Telangiectasia. Sources: Expert Review Amber,Literature non-coding gene tags were added to gene: DROSHA. Mode of inheritance for gene: DROSHA was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: DROSHA were set to 39654947; 35405010; 29339534 Phenotypes for gene: DROSHA were set to Neurodevelopmental disorder, MONDO:0700092; hereditary hemorrhagic telangiectasia MONDO:0019180; idiopathic spontaneous coronary artery dissection MONDO:0007385 |
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