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: Vertigo (D014717)
..Starting node ..Vertigo, Benign Recurrent, 1 (C567620)
Child Nodes:
Sister 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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11590
Name:	Vertigo, Benign Recurrent, 1
Definition:
Alternative IDs:
ParentIDs:	MESH:D014717
TreeNumbers:	C09.218.568.900.883/C567620 \|C10.597.951/C567620 \|C23.888.592.958/C567620
Synonyms:
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: C567620 MeSH: C567620 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants