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 (C562859)
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:

11589

Name:

Vertigo, Benign Recurrent

Definition:

Alternative IDs:

ParentIDs:

MESH:D014717

TreeNumbers:

C09.218.568.900.883/C562859 |C10.597.951/C562859 |C23.888.592.958/C562859

Synonyms:

Slim Mappings:

Ear-nose-throat disease|Nervous system disease|Signs and symptoms

Reference:

MedGen: C562859
MeSH: C562859
OMIM: 193007;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0002141	Gait imbalance
3	HP:0003677	Slowly progressive
4	HP:0002321	Vertigo

Disease Causing ClinVar Variants