Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

optic nerve neoplasm
Synonyms

second cranial nerve tumor

neoplasm of optic nerve (disorder)

second cranial nerve tumour

Optic Nerve Neoplasms

optic nerve tumour

second cranial nerve neoplasm

tumor of the second cranial nerve

tumor of second cranial nerve

second cranial nerve neoplasms

tumour of second cranial nerve

cranial nerve II tumor

cranial nerve II neoplasm (disease)

cranial nerve II tumour

neoplasm of optic nerve

tumor of the optic nerve

tumor of Second Cranial nerve

Tumour of optic nerve

tumour of optic nerve

optic nerve tumor

tumor of optic nerve

neoplasms, optic nerve

tumor of cranial nerve II

neoplasm of second cranial nerve

neoplasm of the optic nerve

tumour of the optic nerve

tumour of cranial nerve II

neoplasm of the second cranial nerve

optic nerve neoplasm

optic nerve neoplasms

tumour of the second cranial nerve

neoplasms, second cranial nerve

cranial nerve II neoplasm

neoplasm of cranial nerve II

cranial nerve II neoplasms

Definitions

Benign and malignant neoplasms which arise from or metastasize to the optic or second cranial nerve which extends from the optic disk of the eye and joins the optic chiasm. Clinical features may include visual loss, proptosis, and local pain. The majority of optic nerve tumors or optic gliomas. Benign and malignant neoplasms that arise from the optic nerve or its sheath. OPTIC NERVE GLIOMA is the most common histologic type. Optic nerve neoplasms tend to cause unilateral visual loss and an afferent pupillary defect and may spread via neural pathways to the brain.

ID

http://www.ebi.ac.uk/efo/EFO_1001073

database_cross_reference

MEDGEN:101181

SCTID:395505000

UMLS:C0524802

MedDRA:10053645

MeSH:D019574

MESH:D019574

MONDO:0002640

SNOMEDCT:395505000

DOID:3419

ICD9:239.7

NCIT:C4801

NCIt:C4801

definition

Benign and malignant neoplasms which arise from or metastasize to the optic or second cranial nerve which extends from the optic disk of the eye and joins the optic chiasm. Clinical features may include visual loss, proptosis, and local pain. The majority of optic nerve tumors or optic gliomas.

Benign and malignant neoplasms that arise from the optic nerve or its sheath. OPTIC NERVE GLIOMA is the most common histologic type. Optic nerve neoplasms tend to cause unilateral visual loss and an afferent pupillary defect and may spread via neural pathways to the brain.

has_exact_synonym

second cranial nerve tumor

neoplasm of optic nerve (disorder)

second cranial nerve tumour

Optic Nerve Neoplasms

optic nerve tumour

second cranial nerve neoplasm

tumor of the second cranial nerve

tumor of second cranial nerve

second cranial nerve neoplasms

tumour of second cranial nerve

cranial nerve II tumor

cranial nerve II neoplasm (disease)

cranial nerve II tumour

neoplasm of optic nerve

tumor of the optic nerve

tumor of Second Cranial nerve

Tumour of optic nerve

tumour of optic nerve

optic nerve tumor

tumor of optic nerve

neoplasms, optic nerve

tumor of cranial nerve II

neoplasm of second cranial nerve

neoplasm of the optic nerve

tumour of the optic nerve

tumour of cranial nerve II

neoplasm of the second cranial nerve

optic nerve neoplasm

optic nerve neoplasms

tumour of the second cranial nerve

neoplasms, second cranial nerve

cranial nerve II neoplasm

neoplasm of cranial nerve II

cranial nerve II neoplasms

id

EFO:1001073

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

label

optic nerve neoplasm

notation

EFO:1001073

preferred label

optic nerve neoplasm

prefLabel

optic nerve neoplasm

skos_exactMatch

http://identifiers.org/snomedct/395505000

http://purl.obolibrary.org/obo/EFO_1001073

http://identifiers.org/mesh/D019574

http://linkedlifedata.com/resource/umls/id/C0524802

http://purl.obolibrary.org/obo/DOID_3419

http://purl.obolibrary.org/obo/NCIT_C4801

http://identifiers.org/medgen/101181

term editor

Sirarat Sarntivijai

subClassOf

http://purl.obolibrary.org/obo/MONDO_0002135

http://www.ebi.ac.uk/efo/EFO_0003833

http://www.ebi.ac.uk/efo/EFO_0000616

http://purl.obolibrary.org/obo/MONDO_0002633

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