Disease browser and phenotype portal

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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: Neurologic Manifestations (D009461)
Parent Node: Vestibular Diseases (D015837)
..Starting node ..Vertigo (D014717)
Child Nodes:
........Benign Paroxysmal Positional Vertigo (D065635)
........Episodic Ataxia, Type 3 (C564697)
........Vertigo, Benign Recurrent (C562859)
........Vertigo, Benign Recurrent, 1 (C567620)
........Vertigo, Benign Recurrent, 2 (C567749)
Sister Nodes:
..Kabuki syndrome (C537705)
..Vertigo (D014717) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11588
Name:	Vertigo
Definition:	An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1)
Alternative IDs:
ParentIDs:	MESH:D009461\|MESH:D015837
TreeNumbers:	C09.218.568.900.883 \|C10.597.951 \|C23.888.592.958
Synonyms:	Brainstem Vertigo \|Brain Stem Vertigo \|Brainstem Vertigos \|Brain Stem Vertigos \|Central Nervous System Origin Vertigo \|Central Origin Vertigo \|Central Origin Vertigos \|CNS Origin Vertigo \|CNS Origin Vertigos \|Constant Vertigo \|Constant Vertigos \|Essential Vertigo \|E
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: D014717 MeSH: D014717 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants