Skip to main content
Diseases

Nerve Optic Tumor

nerve optic tumor

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Nerve Optic Tumor
Standard Disease Name
nerve optic tumor
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D019574
OMIM ID
No data
UMLS ID
C0524802
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:Benign and malignant neoplasms which arise from or metastasize to the optic or second cranial nerve which extends from the optic disc 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.|MSH2017_2016_08_12: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.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ACE
angiotensin I converting enzyme
angiotensin I converting enzyme
02
CDKN2A
cyclin dependent kinase inhibitor 2A
cyclin dependent kinase inhibitor 2A
05
MAP2
microtubule associated protein 2
microtubule associated protein 2