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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Cranial Nerve Diseases (D003389)
Parent Node: Retrocochlear Diseases (D012181)
..Starting node ..Vestibulocochlear Nerve Diseases (D000160)
Child Nodes:
........Cogan Syndrome (D055952) 2
........Deafness, X-Linked 5 (C564472)
........Neuroma, Acoustic (D009464) 1
........Vestibular Neuronitis (D020338)
........Vestibulocochlear Dysfunction, Progressive (C536346)
........Vestibulocochlear Nerve Injuries (D061285)
Sister Nodes:
..Auditory Diseases, Central (D001304) 19
..Vestibulocochlear Nerve Diseases (D000160) 9
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11602
Name:	Vestibulocochlear Nerve Diseases
Definition:	Pathological processes of the VESTIBULOCOCHLEAR NERVE, including the branches of COCHLEAR NERVE and VESTIBULAR NERVE. Common examples are VESTIBULAR NEURITIS, cochlear neuritis, and ACOUSTIC NEUROMA. Clinical signs are varying degree of HEARING LOSS; VERTIGO; and TINNITUS.
Alternative IDs:
ParentIDs:	MESH:D003389\|MESH:D012181
TreeNumbers:	C09.218.807.800 \|C10.292.910
Synonyms:	Acoustic Nerve Disease \|Acoustic Nerve Diseases \|Acoustic Nerve Disorder \|Acoustic Nerve Disorders \|Cochlear Nerve Disease \|Cochlear Nerve Diseases \|Cochlear Nerve Disorder \|Cochlear Nerve Disorders \|Cochlear Neuritides \|Cochlear Neuritis \|Cranial Nerve VIII Disea
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease
Reference:	MedGen: D000160 MeSH: D000160 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants