Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Optic Nerve Diseases » Optic Nerve Hypoplasia
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Optic Nerve Hypoplasia
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Optic Nerve Hypoplasia
Diseases [C] » Eye Diseases [C11] » Optic Nerve Diseases » Optic Nerve Hypoplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Optic Nerve Hypoplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Optic Nerve Hypoplasia
Description
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. MeSH
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Subtype Terms (1)
Septo-Optic Dysplasia
1 approved drug
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UMLS Data
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