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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: Corneal Diseases (D003316)
..Starting node ..Corneal Edema (D015715)
Child Nodes:
Sister Nodes:
..Arnold Stickler Bourne syndrome (C537431)
..Cataract microcornea syndrome (C538287)
..Cornea Plana 1 (C565158)
..Cornea Plana 2 (C565677)
..Corneal Dystrophies, Hereditary (D003317) 61
..Corneal Edema (D015715)
..Corneal Endothelial Cell Loss (D055954)
..Corneal hypesthesia, familial (C536440)
..Corneal Injuries (D065306) 1
..Corneal Neovascularization (D016510)
..Corneal Opacity (D003318) 10
..Corneal Wavefront Aberration (D057108)
..Dermoids of cornea (C535376)
..Iridocorneal Endothelial Syndrome (D057129)
..Keratitis (D007634) 14
..Keratoconus (D007640) 9
..Macrophthalmia, Colobomatous, with Microcornea (C566533)
..Microspherophakia (C563255)
..Neuhauser syndrome (C536143)
..Ramos Arroyo Clark syndrome (C535286)
..Ring dermoid of cornea (C535684)
..Sclerocornea (C565209)
..Sclerocornea, Autosomal Dominant (C566692)
..Stern Lubinsky Durrie syndrome (C537488)
..Trachoma (D014141)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2738
Name:	Corneal Edema
Definition:	An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity.
Alternative IDs:
ParentIDs:	MESH:D003316
TreeNumbers:	C11.204.267
Synonyms:	Corneal Edemas \|Edema, Corneal \|Edemas, Corneal
Slim Mappings:	Eye disease
Reference:	MedGen: D015715 MeSH: D015715 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants