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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: Eye Infections, Viral (D015828)
Parent Node: Herpes Simplex (D006561)
Parent Node: Keratitis (D007634)
..Starting node ..Keratitis, Herpetic (D016849)
Child Nodes:
........Keratitis, Dendritic (D007635)
Sister Nodes:
..Acanthamoeba Keratitis (D015823)
..Corneal Ulcer (D003320) 1
..Dermatoosteolysis Kirghizian type (C535373)
..Keratitis Fugax Hereditaria (C563650)
..Keratitis, hereditary (C537022)
..Keratitis, Herpetic (D016849) 1
..Keratitis, Ichthyosis, and Deafness (KID) Syndrome (C536168)
..Keratitis-Ichthyosis-Deafness Syndrome (C580224)
..Keratoconjunctivitis (D007637) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6045
Name:	Keratitis, Herpetic
Definition:	A superficial, epithelial Herpesvirus hominis infection of the cornea, characterized by the presence of small vesicles which may break down and coalesce to form dendritic ulcers (KERATITIS, DENDRITIC). (Dictionary of Visual Science, 3d ed)
Alternative IDs:
ParentIDs:	MESH:D006561\|MESH:D007634\|MESH:D015828
TreeNumbers:	C02.256.466.382.465 \|C02.325.465 \|C11.204.564.425 \|C11.294.800.475
Synonyms:	Herpes Simplex Keratitides \|Herpes Simplex Keratitis \|Herpes Simplex, Ocular \|Herpetic Keratitides \|Herpetic Keratitis \|Keratitides, Herpes Simplex \|Keratitides, Herpetic \|Keratitis, Herpes Simplex \|Ocular Herpes Simplex
Slim Mappings:	Eye disease\|Viral disease
Reference:	MedGen: D016849 MeSH: D016849 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants