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:0008031 | HP:0008031 | Posterior Y-sutural cataract | 0 | CRYBA1 CL E G H | 1411 | 2394 | OMIM:600881 | Cataract, congenital zonular, with sutural opacities | . | | | 9 | | |
HP:0008031 | HP:0008031 | Posterior Y-sutural cataract | 0 | NHS CL E G H | 4810 | 7820 | OMIM:302350 | Nance-Horan syndrome | . | | | 88 | | |
HP:0008031 | HP:0008031 | Posterior Y-sutural cataract | 0 | SEC23A CL E G H | 10484 | 10701 | ORPHA:50814 | Craniolenticulosutural dysplasia | HP:0040281 - Very frequent | | | 2 | | |
HP:0008031 | HP:0008031 | Posterior Y-sutural cataract | 0 | SEC23A CL E G H | 10484 | 10701 | OMIM:607812 | Craniolenticulosutural dysplasia | | | | 2 | | |