Disease Browser
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Parent Node: Fuchs' Endothelial Dystrophy (D005642) | ..Starting node ..Corneal Dystrophy, Fuchs Endothelial, 5 (C567676)
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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)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2724 |
Name: | Corneal Dystrophy, Fuchs Endothelial, 5 |
Definition: | |
Alternative IDs: | OMIM:613269 |
ParentIDs: | MESH:D005642 |
TreeNumbers: | C11.204.236.438/C567676 |C11.270.162.438/C567676 |C16.320.290.162.410/C567676 |
Synonyms: | CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET |FCD3 LOCUS |FECD5 |
Slim Mappings: | Eye disease|Genetic disease (inborn) |
Reference: |
MedGen: C567676
MeSH: C567676
OMIM: 613269;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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