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: Rubivirus Infections (D018355)
..Starting node ..Rubella (D012409)
Child Nodes:
........Rubella Syndrome, Congenital (D012410)
Sister Nodes:
..Rubella (D012409) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9913
Name:	Rubella
Definition:	An acute infectious disease caused by the RUBELLA VIRUS. The virus enters the respiratory tract via airborne droplet and spreads to the LYMPHATIC SYSTEM.
Alternative IDs:
ParentIDs:	MESH:D018355
TreeNumbers:	C02.782.930.700.700
Synonyms:	German Measles \|Measles, German \|Measles, Three Day \|Measle, Three Day \|Rubellas \|Three Day Measle \|Three Day Measles
Slim Mappings:	Viral disease
Reference:	MedGen: D012409 MeSH: D012409 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants