Optic Atrophies, Hereditary D015418

Related MeSH Hierarchy (6)

Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Optic Nerve Diseases » Optic Atrophy » Optic Atrophies, Hereditary

Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System » Optic Atrophies, Hereditary

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

Diseases [C] » Eye Diseases [C11] » Optic Nerve Diseases » Optic Atrophy » Optic Atrophies, Hereditary

Description

Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).   MeSH

Subtype Terms (3)

Optic Atrophy, Hereditary, Leber
18 drugs (2 approved, 16 experimental)

Wolfram Syndrome
6 approved drugs


Organization Involved with Phase 3 Indications (1)

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UMLS Data


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