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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: Labyrinth Diseases (D007759)
..Starting node ..Vestibular Diseases (D015837)
Child Nodes:
........Kabuki syndrome (C537705)
........Vertigo (D014717) 5
Sister Nodes:
..Cochlear Diseases (D015834)
..Endolymphatic Hydrops (D018159) 1
..Labyrinthitis (D007762)
..Vestibular Diseases (D015837) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11599
Name:	Vestibular Diseases
Definition:	Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls.
Alternative IDs:
ParentIDs:	MESH:D007759
TreeNumbers:	C09.218.568.900
Synonyms:	Diseases, Vestibular \|Disease, Vestibular \|Vestibular Disease
Slim Mappings:	Ear-nose-throat disease
Reference:	MedGen: D015837 MeSH: D015837 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants