| Nail-Patella Syndrome via the LMX1B Gene |
Ne32029 |
مشاهده
|
| Leber's Hereditary Optic Neuropathy |
32027 |
مشاهده
|
| Retinitis Pigmentosa |
32032 |
مشاهده
|
| Achromatopsia (ACHM) |
3201 |
مشاهده
|
| Oculocutaneous Albinism (OCA) |
32030 |
مشاهده
|
| Alport Syndrome |
Op3202 |
مشاهده
|
| Microphthalmia.Anophthalmia.Coloboma |
386495000 |
مشاهده
|
| Anterior Segment Dysgenesis Disorders |
3203 |
مشاهده
|
| Ataxia .with Oculomotor Apraxia |
Op3204 |
مشاهده
|
| Axenfeld-Rieger Syndrome |
Op3207 |
مشاهده
|
| Brittle Cornea Syndrome |
3208 |
مشاهده
|
| Comprehensive Cataracts |
32011 |
مشاهده
|
| Congenital Cataracts |
32016 |
مشاهده
|
| Comprehensive Ocular Disorders |
32013 |
مشاهده
|
| Cone-Rod Dystrophy |
32015 |
مشاهده
|
| Corneal Dystrophies |
32115 |
مشاهده
|
| Cystinosis via the CTNS Gene |
Op32018 |
مشاهده
|
| Strabismus Syndrome or Congenital Fibrosis of Extraocular Muscles (Ocular Motility Disorder) |
32037 |
مشاهده
|
| Flecked Retina Disorder |
32020 |
مشاهده
|
| Glaucoma |
32022 |
مشاهده
|
| Hermansky-Pudlak Syndrome (HPS) |
32023 |
مشاهده
|
| Inherited Platelet Function Disorder |
32025 |
مشاهده
|
| Hypopigmentation |
32024 |
مشاهده
|
| Leber Congenital Amaurosis |
32026 |
مشاهده
|
| Stargardt Disease (STGD) and Macular Dystrophies |
32035 |
مشاهده
|
| Early-Onset High Myopia |
32019 |
مشاهده
|
| Congenital Stationary Night Blindness |
32017 |
مشاهده
|
| Chronic Progressive External Ophthalmoplegia |
Op3209 |
مشاهده
|
| Optic Atrophy |
32031 |
مشاهده
|
| Autosomal Dominant Retinitis Pigmentosa (RP) |
3205 |
مشاهده
|
| Autosomal Recessive Retinitis Pigmentosa (RP) |
3206 |
مشاهده
|
| Comprehensive Inherited Retinal Dystrophies |
32012 |
مشاهده
|
| Focused Inherited Retinal Disorders |
32021 |
مشاهده
|
| Retinitis .Pigmentosa |
32032 |
مشاهده
|
| X-linked Retinitis Pigmentosa (XLRP) and Choroideremia |
32042 |
مشاهده
|
| Septo.optic Dysplasia Spectrum |
Op32034 |
مشاهده
|
| COL2A1.Related Disorders via the COL2A1 Gene |
Op32010 |
مشاهده
|
| Stickler Syndrome |
Op32036 |
مشاهده
|
| Usher Syndrome |
Op3182 |
مشاهده
|
| Comprehensive Vitreoretinopathy |
32014 |
مشاهده
|
| Warburg .Micro Syndrome |
Op32039 |
مشاهده
|
| WFS1-Related Disorders via the WFS1 |
Op32040 |
مشاهده
|
| Wolfram Syndrome |
Op32041 |
مشاهده
|
| Xeroderma Pigmentosum (XP) |
Op31162 |
مشاهده
|