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Septo-Optic Dysplasia MeSH Descriptor Data 2022


MeSH Heading
Septo-Optic Dysplasia
Tree Number(s)
C10.500.034.937
C10.500.760.500
C16.131.666.034.937
C16.131.666.763.500
Unique ID
D025962
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D025962
Scope Note
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.
Entry Term(s)
De Morsier Syndrome
Septo-Optic Dysplasia with Growth Hormone Deficiency
Septooptic Dysplasia
Previous Indexing
Hypogonadism (1966-1971)
Optic Nerve (1972-2001)
Septum Pellucidum (1972-2001)
Public MeSH Note
2002
History Note
2002
Date Established
2002/01/01
Date of Entry
2001/07/25
Revision Date
2021/02/09
Septo-Optic Dysplasia Preferred
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