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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: Abnormalities, Multiple (D000015)
Parent Node: Rubella (D012409)
..Starting node ..Rubella Syndrome, Congenital (D012410)
Child Nodes:
Sister Nodes:
..Rubella Syndrome, Congenital (D012410)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9914
Name:	Rubella Syndrome, Congenital
Definition:	Transplacental infection of the fetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalized growth retardation. (From Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D000015\|MESH:D012409
TreeNumbers:	C02.782.930.700.700.700 \|C16.131.077.790
Synonyms:	Congenital Rubella Syndrome \|Congenital Rubella Syndromes \|Rubella Syndromes, Congenital \|Syndrome, Congenital Rubella \|Syndromes, Congenital Rubella
Slim Mappings:	Congenital abnormality\|Viral disease
Reference:	MedGen: D012410 MeSH: D012410 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants