| Descriptor English: | Septo-Optic Dysplasia | ||||||
| Descriptor Spanish: |
Displasia Septo-Óptica
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| Descriptor Portuguese: | Displasia Septo-Óptica | ||||||
| Descriptor French: | Dysplasie septo-optique | ||||||
| Entry term(s): |
De Morsier Syndrome Dysplasia, Septooptic Dysplasias, Septooptic Septo Optic Dysplasia with Growth Hormone Deficiency Septo-Optic Dysplasia with Growth Hormone Deficiency Septooptic Dysplasia Septooptic Dysplasias Syndrome, De Morsier |
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| Tree number(s): |
C10.292.562.700.375.875 C10.500.034.937 C10.500.760.500 C11.590.436.400.875 C16.131.666.034.937 C16.131.666.763.500 |
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| RDF Unique Identifier: | https://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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Hypogonadism (1966-1971) Optic Nerve (1972-2001) Septum Pellucidum (1972-2001) |
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| Public MeSH Note: | 2002 |
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| History Note: | 2002 |
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| DeCS ID: | 36013 | ||||||
| Unique ID: | D025962 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2002/01/01 | ||||||
| Date of Entry: | 2001/07/25 | ||||||
| Revision Date: | 2020/01/10 |
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DISEASES
Eye Diseases [C11]Eye Diseases
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Septo-Optic Dysplasia
- Preferred
| Concept UI |
M0376630 |
| 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. |
| Preferred term | Septo-Optic Dysplasia |
| Entry term(s) |
De Morsier Syndrome Dysplasia, Septooptic Dysplasias, Septooptic Septo Optic Dysplasia with Growth Hormone Deficiency Septo-Optic Dysplasia with Growth Hormone Deficiency Septooptic Dysplasia Septooptic Dysplasias Syndrome, De Morsier |
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