Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders » Septo-Optic Dysplasia
Diseases [C] » Eye Diseases [C11] » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders » Septo-Optic Dysplasia
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Agenesis of Corpus Callosum » Septo-Optic Dysplasia
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Optic Nerve Hypoplasia » Septo-Optic Dysplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Agenesis of Corpus Callosum » Septo-Optic Dysplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Optic Nerve Hypoplasia » Septo-Optic Dysplasia
Description
A condition resulting from congenital malformations involving the brain. The syndrome of septo-optic dysplasia combines hypoplasia or agenesis of the SEPTUM PELLUCIDUM; CORPUS CALLOSUM and the OPTIC NERVE. The extent of the abnormalities can vary. Septo-optic dysplasia is often associated with abnormalities of the HYPOTHALAMUS and other diencephalic structures, and HYPOPITUITARISM. MeSH
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Phase 4 Indicated Drugs (1)
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UMLS Data
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