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To save room on the page we use the term disabled to indicate those with disabilities, special need or a medical condition.
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& UK Support Groups 
A page for this condition is in the Contact a Family Directory, it may be able to help you further.
There are conditions similar or related to this one that have people listed against them. They are listed below. If there are UK Support groups available, they will be indicated by this 
icon. Click this icon to view the list of available support groups.
| Condition (also listed as) | No. of members | Support Group |
|---|---|---|
| 3rd Nerve Palsy of the Eye | 2 | - |
| Achromatopsia | 0 | - |
| Acute Zonal Occult Outer Retinopathy (AZOOR) | 0 | - |
| Adie Syndrome (Holmes-Adie Syndrome) | 2 | - |
| Ametropia | 0 | - |
| Aniridia (Congenital Abnormality of the Iris) | 13 | - |
| Anophthalmia (Heminasal Aplasia) | 4 | |
| Axenfeld Syndrome (Axenfeld Anomaly; Axenfeld-Rieger Syndrome; Rieger Syndrome) | 0 | - |
| Axenfeld-Schürenberg Syndrome (Cyclic Oculomotor Paralysis; Congenital Cyclic Oculomotor Paralysis) | 0 | - |
| Cataracts | 20 | |
| Choroideremia | 0 | - |
| Chromotosia Congenita | 0 | - |
| Coats' Disease (Exudative Retinitis) | 8 | - |
| coloboma & cyst on the cerebellum | 0 | - |
| Colourblindness | 0 | - |
| Cone Dystrophy (Combined Cone-Rod Degeneration; Progressive Cone-Rod Degeneration; Cone-Rod Dystrophy; Retinal Cone Degeneration; Retinal Cone Dystrophy; Retinal Cone-Rod Dystrophy) | 1 | - |
| Congenital Stationary Night Blindness | 6 | - |
| Corneal Dystrophy | 5 | - |
| Eales Disease | 1 | - |
| Familial exudative vitreoretinopathy (FEVR) | 2 | - |
| Glaucoma | 10 | |
| Homonymous Hemianopia | 6 | - |
| Idiopathic Optic Atrophy | 1 | - |
| Keratoconus | 2 | |
| Macular Disease | 0 | |
| Macular Dystrophy | 1 | - |
| Microphthalmia | 5 | - |
| Nystagmus (Spasmus nutans,Congenital Idiopathic Nystagmus) | 21 | |
| Nystagmus and Astigmatism | 7 | - |
| Ocular Disorders (Drusen Syndrome) | 0 | - |
| Optic Nerve Atrophy | 6 | - |
| Optic Nerve Dysplasia | 2 | - |
| Optic Nerve Hypoplasia | 20 | - |
| Persistant Hyperplastic Primary Vitreous | 2 | - |
| Peter's Anomaly | 7 | - |
| Peter's Plus Syndrome (Peter's Plus Anomaly) | 11 | - |
| Pigment Epithelium retinal detachment | 0 | - |
| Post Polymorhous Corneal Dystrophy | 0 | - |
| Reis-Büclers (Reis-Bncklers) | 0 | - |
| Retinitis Pigmentosa (Bulls Eye Dystrophy; Central Areola Choroidal Dystrophy; Retinal Dystrophy, Tapeto Retinal Degenaration) | 2 | |
| Retinopathy of Prematurity | 1 | - |
| Rieger's Anomaly | 1 | - |
| Rod Monochromatisim | 0 | - |
| Sclerocornea | 3 | - |
| Spheromicrophakia | 0 | - |
| Thyroid Eye Disease (Thyroid Ophthalmopathy; Thyroid Associated Ophthalmopathy; Graves' Eye Disease; Graves' Ophthalmopathy ) | 1 | |
| Uveitis | 1 | |
