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:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | ATOH7 CL E G H | 220202 | 13907 | OMIM:221900 | Persistent hyperplastic primary vitreous, autosomal recessive | . | | | 4 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | CYP1B1 CL E G H | 1545 | 2597 | OMIM:617315 | ANTERIOR SEGMENT DYSGENESIS 6; ASGD6 | | | | 101 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | FOXC1 CL E G H | 2296 | 3800 | OMIM:602482 | Axenfeld-rieger syndrome, type 3 | | | | 63 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | FOXE3 CL E G H | 2301 | 3808 | OMIM:610256 | Anterior segment dysgenesis 2 | . | | | 23 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | HMX1 CL E G H | 3166 | 5017 | OMIM:612109 | Oculoauricular syndrome | | | | 2 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | LCA5 CL E G H | 167691 | 31923 | ORPHA:364055 | Severe early-childhood-onset retinal dystrophy | HP:0040283 - Occasional | | | 70 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | LRAT CL E G H | 9227 | 6685 | ORPHA:364055 | Severe early-childhood-onset retinal dystrophy | HP:0040283 - Occasional | | | 62 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | MIR204 CL E G H | 406987 | 31582 | OMIM:616722 | Retinal dystrophy and iris coloboma with or without congenital cataract | . | | | 1 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | RPE65 CL E G H | 6121 | 10294 | ORPHA:364055 | Severe early-childhood-onset retinal dystrophy | HP:0040283 - Occasional | | | 129 | | |
HP:0011484 | HP:0011484 | Posterior synechiae of the anterior chamber | 0 | SPATA7 CL E G H | 55812 | 20423 | ORPHA:364055 | Severe early-childhood-onset retinal dystrophy | HP:0040283 - Occasional | | | 48 | | |