Käsitteen tiedot
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Agenesis of Corpus Callosum
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Agenesis of Corpus Callosum
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Optic Nerve Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Nerve Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Congenital Cranial Dysinnervation Disorders
Eye Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Congenital Cranial Dysinnervation Disorders
Käytettävä termi
Septo-Optic Dysplasia
Tyyppi
-
Topical Descriptor
Yläkäsite
Ohjaustermit
- De Morsier Syndrome
- Dysplasia, Septooptic
- Septooptic Dysplasia
- Septooptic Dysplasias
- Septo Optic Dysplasia with Growth Hormone Deficiency
- Septo-Optic Dysplasia with Growth Hormone Deficiency
Käyttöhuomautus
- 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.
Huomautus muutoshistoriasta
- 2002
Muunkieliset termit
-
ruotsi
-
suomi
-
dysplasia septo-optica
URI
http://www.yso.fi/onto/mesh/D025962
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