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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: Dystonia (D004421)
Parent Node: Optic Atrophy, Hereditary, Leber (D029242)
..Starting node ..Marsden syndrome (C536024)
Child Nodes:
Sister Nodes:
..Marsden syndrome (C536024)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6801
Name:	Marsden syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D004421\|MESH:D029242
TreeNumbers:	C10.292.700.225.500.400/C536024 \|C10.574.500.662.400/C536024 \|C10.597.350.300/C536024 \|C11.270.564.400/C536024 \|C11.640.451.451.400/C536024 \|C16.320.290.564.400/C536024 \|C16.320.400.630.400/C536024 \|C18.452.660.670/C536024 \|C23.888.592.350.300/C536024
Synonyms:	Dystonia, familial, with visual failure and striatal lucencies \|Leber Hereditary Optic Neuropathy With Dystonia
Slim Mappings:	Eye disease\|Genetic disease (inborn)\|Metabolic disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: C536024 MeSH: C536024 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants