Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | BAP1 CL E G H | 8314 | 950 | ORPHA:39044 | Uveal melanoma | HP:0040283 - Occasional | | | 184 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | BEST1 CL E G H | 7439 | 12703 | OMIM:193220 | VITREORETINOCHOROIDOPATHY | . | | | 182 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | CAPN5 CL E G H | 726 | 1482 | OMIM:193235 | Vitreoretinopathy, neovascular inflammatory | . | | | 6 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | CTNNB1 CL E G H | 1499 | 2514 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 88 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | CYSLTR2 CL E G H | 57105 | 18274 | ORPHA:39044 | Uveal melanoma | HP:0040283 - Occasional | | | 1 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | FZD4 CL E G H | 8322 | 4042 | OMIM:133780 | Exudative vitreoretinopathy 1 | . | | | 109 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | FZD4 CL E G H | 8322 | 4042 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 109 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | FZD4 CL E G H | 8322 | 4042 | ORPHA:90050 | Retinopathy of prematurity | HP:0040283 - Occasional | | | 109 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | GNA11 CL E G H | 2767 | 4379 | ORPHA:39044 | Uveal melanoma | HP:0040283 - Occasional | | | 16 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | GNAQ CL E G H | 2776 | 4390 | ORPHA:39044 | Uveal melanoma | HP:0040283 - Occasional | | | 7 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | LRP5 CL E G H | 4041 | 6697 | OMIM:133780 | Exudative vitreoretinopathy 1 | . | | | 125 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | LRP5 CL E G H | 4041 | 6697 | OMIM:601813 | Exudative vitreoretinopathy 4 | . | | | 125 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | LRP5 CL E G H | 4041 | 6697 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 125 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | LRP5 CL E G H | 4041 | 6697 | ORPHA:90050 | Retinopathy of prematurity | HP:0040283 - Occasional | | | 125 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | NDP CL E G H | 4693 | 7678 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 39 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | NDP CL E G H | 4693 | 7678 | ORPHA:90050 | Retinopathy of prematurity | HP:0040283 - Occasional | | | 39 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | PROC CL E G H | 5624 | 9451 | OMIM:612304 | Thrombophilia due to protein C deficiency, autosomal recessive | . | | | 65 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | RB1 CL E G H | 5925 | 9884 | OMIM:180200 | RETINOBLASTOMA | . | | | 365 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | RS1 CL E G H | 6247 | 10457 | OMIM:312700 | Retinoschisis 1, X-linked, juvenile | | | | 148 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | SF3B1 CL E G H | 23451 | 10768 | ORPHA:39044 | Uveal melanoma | HP:0040283 - Occasional | | | 19 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | TSPAN12 CL E G H | 23554 | 21641 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 39 | | |
HP:0007902 | HP:0007902 | Vitreous hemorrhage | 0 | ZNF408 CL E G H | 79797 | 20041 | ORPHA:891 | Familial exudative vitreoretinopathy | HP:0040283 - Occasional | | | 14 | | |