MeSH Browser

MeSH Heading: Optic Nerve Diseases
Tree Number(s): C10.292.700; C11.640
Unique ID: D009901
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D009901
Annotation: SMON: see note on OPTIC NEURITIS; inflamm dis = OPTIC NEURITIS
Scope Note: Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect.
Entry Version: OPTIC NERVE DIS
Entry Term(s): Cranial Nerve II Diseases; Cranial Nerve II Disorder; Foster-Kennedy Syndrome; Neural-Optical Lesion; Optic Disc Disorders; Optic Disk Disorders; Optic Neuropathy; Second Cranial Nerve Diseases
NLM Classification #: WW 280
Previous Indexing: Optic Nerve (1966-1975)
Public MeSH Note: 76
History Note: 76; was NON MESH before 1976
Date Established: 1976/01/01
Date of Entry: 1975/07/25
Revision Date: 2019/04/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0015358
Scope Note: Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect.
Terms: Optic Nerve Diseases Preferred Term
Term UI T029321
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1976); Neural-Optical Lesion
Term UI T029320
Date12/26/1978
LexicalTag NON
ThesaurusID UNK (19XX); Cranial Nerve II Diseases
Term UI T370670
Date11/04/1999
LexicalTag NON
ThesaurusID NLM (2000); Optic Neuropathy
Term UI T370671
Date11/04/1999
LexicalTag NON
ThesaurusID NLM (2000); Second Cranial Nerve Diseases
Term UI T370672
Date11/04/1999
LexicalTag NON
ThesaurusID NLM (2000); Cranial Nerve II Disorder
Term UI T370673
Date11/04/1999
LexicalTag NON
ThesaurusID NLM (2000)

Optic Nerve Diseases MeSH Descriptor Data 2024