Eye Diseases, Hereditary D015785

Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary

Description

Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.   MeSH

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Subtype Terms (23)

Aicardi Syndrome
5 approved drugs

Albinism
6 drugs (4 approved, 2 experimental)

Aniridia
1 experimental drug

Choroideremia
7 drugs (2 approved, 5 experimental)

Coloboma
 

Cone Dystrophy
 

Cone-Rod Dystrophies
1 experimental drug

Corneal Dystrophies, Hereditary
3 drugs (2 approved, 1 experimental)

Duane Retraction Syndrome
 

Familial Exudative Vitreoretinopathies
1 approved drug

Graves Ophthalmopathy
50 drugs (38 approved, 12 experimental)

Gyrate Atrophy
 

Leber Congenital Amaurosis
12 drugs (5 approved, 7 experimental)

Optic Atrophies, Hereditary
 

Optic Nerve Hypoplasia
1 experimental drug

Retinal Degeneration
24 drugs (7 approved, 17 experimental)

Retinal Dysplasia
 

Retinitis Pigmentosa
58 drugs (17 approved, 41 experimental)

Retinoblastoma
54 drugs (33 approved, 21 experimental)

Stargardt Disease
11 drugs (3 approved, 8 experimental)

Vitelliform Macular Dystrophy
1 approved drug

Walker-Warburg Syndrome
 

Weill-Marchesani Syndrome
 


Phase 3 Indicated Drugs (2)

Other Experimental Indicated Drugs (4)


Organization Involved with Phase 3 Indications (1)

Organization Involved with Other Experimental Indications (1)

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UMLS Data


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