Loading disease data
| Disease | Prevalence | Drugs | Proteins | |
|---|---|---|---|---|
| Macular degeneration, age-related, 14 (ARMD14) | N/A | 78 | 2 | |
| Cataract 30, multiple types (CTRCT30) | N/A | 46 | 1 | |
| Cataract 9, multiple types (CTRCT9) | N/A | — | 1 | |
| Corneal dystrophy, Avellino type (CDA) | N/A | — | 1 | |
| Corneal dystrophy, congenital stromal (CSCD) | Ultra-Rare | — | 1 | |
| Corneal dystrophy, epithelial basement membrane (EBMD) | N/A | — | 1 | |
| Corneal dystrophy, Groenouw type 1 (CDGG1) | N/A | — | 1 | |
| Corneal dystrophy, lattice type 1 (CDL1) | N/A | — | 1 | |
| Corneal dystrophy, lattice type 3A (CDL3A) | N/A | — | 1 | |
| Corneal dystrophy, Reis-Bucklers type (CDRB) | Ultra-Rare | — | 1 | |
| Corneal dystrophy, Thiel-Behnke type (CDTB) | N/A | — | 1 | |
| Developmental and epileptic encephalopathy 117 (DEE117) | Very Rare | 4 | 1 | |
| Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3) | Rare | — | 1 | |
| Glaucoma 1, open angle, A (GLC1A) | Rare | — | 1 | |
| Glaucoma 1, open angle, E (GLC1E) | N/A | 42 | 1 | |
| Glaucoma 1, open angle, P (GLC1P) | N/A | 42 | 1 | |
| Glaucoma 3, primary congenital, A (GLC3A) | Rare | — | 1 | |
| Glaucoma, normal pressure (NPG) | N/A | — | 1 | |
| Hyperferritinemia with or without cataract (HRFTC) | Ultra-Rare | — | 1 | |
| Microphthalmia, syndromic, 1 (MCOPS1) | N/A | — | 1 | |
| Microphthalmia, syndromic, 3 (MCOPS3) | Ultra-Rare | — | 1 | |
| Microphthalmia/Coloboma 10 (MCOPCB10) | Uncommon | — | 1 | |
| Microphthalmia/coloboma and skeletal dysplasia syndrome (MCSKS) | Ultra-Rare | — | 1 | |
| Night blindness, congenital stationary, autosomal dominant 2 (CSNBAD2) | N/A | — | 1 | |
| Osteopetrosis, autosomal recessive 2 (OPTB2) | Very Rare | — | 1 | |
| Osteopetrosis, autosomal recessive 3 (OPTB3) | Ultra-Rare | — | 1 | |
| Piebald trait (PBT) | N/A | — | 1 | |
| Vitreoretinopathy, exudative 7 (EVR7) | N/A | 1 | 1 |