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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: Fuchs' Endothelial Dystrophy (D005642)
..Starting node ..Corneal Dystrophy, Fuchs Endothelial, 7 (C567674)
Child Nodes:
Sister Nodes:
..Cornea guttata with anterior polar cataract (C535471)
..Corneal Dystrophy, Fuchs Endothelial, 3 (C567678)
..Corneal Dystrophy, Fuchs Endothelial, 4 (C567677)
..Corneal Dystrophy, Fuchs Endothelial, 5 (C567676)
..Corneal Dystrophy, Fuchs Endothelial, 6 (C567675)
..Corneal Dystrophy, Fuchs Endothelial, 7 (C567674)
..Corneal dystrophy, Fuchs' endothelial, 1 (C535478)
..Corneal dystrophy, Fuchs' endothelial, 2 (C535479)
..Corneal endothelial dystrophy type 2 (C536439)
..Fuchs atrophia gyrata chorioideae et retinae (C538071)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2726
Name:	Corneal Dystrophy, Fuchs Endothelial, 7
Definition:
Alternative IDs:	OMIM:613271
ParentIDs:	MESH:D005642
TreeNumbers:	C11.204.236.438/C567674 \|C11.270.162.438/C567674 \|C16.320.290.162.410/C567674
Synonyms:	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET \|FCD4 LOCUS \|FECD7
Slim Mappings:	Eye disease\|Genetic disease (inborn)
Reference:	MedGen: C567674 MeSH: C567674 OMIM: 613271; Genes:
Phenotypes
Disease Causing ClinVar Variants