Optic Nerve Hypoplasia

A group of rare genetic disorders characterized by underdeveloped OPTIC NERVES, resulting in increased incidences of vision impairment, CONGENITAL NYSTAGMUS and STRABISMUS. It may be syndromic, and is often associated with CNS malformations.

Year introduced: 2020

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Tree Number(s): C10.292.700.463, C10.500.760, C11.270.588, C11.640.522, C16.131.666.763, C16.320.290.612

MeSH Unique ID: D000080344

Entry Terms:

• Hypoplasia, Optic Nerve
• Superior Segmental Optic Nerve Hypoplasia
• Superior Segmental Optic Hypoplasia

Previous Indexing:

• Optic Nerve/abnormalities (1969-2019)

All MeSH Categories
Diseases Category
Nervous System Diseases
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Nerve Hypoplasia

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Optic Nerve Hypoplasia
Septo-Optic Dysplasia

All MeSH Categories
Diseases Category
Eye Diseases
Eye Diseases, Hereditary
Optic Nerve Hypoplasia

All MeSH Categories
Diseases Category
Eye Diseases
Optic Nerve Diseases
Optic Nerve Hypoplasia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Optic Nerve Hypoplasia
Septo-Optic Dysplasia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Nerve Hypoplasia