Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Conjunctivitis (D003231)
Parent Node: Keratitis (D007634)
..Starting node ..Keratoconjunctivitis (D007637)
Child Nodes:
........Keratoconjunctivitis Sicca (D007638) 1
........Keratoconjunctivitis, Infectious (D007639)
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:	6051
Name:	Keratoconjunctivitis
Definition:	Simultaneous inflammation of the cornea and conjunctiva.
Alternative IDs:
ParentIDs:	MESH:D003231\|MESH:D007634
TreeNumbers:	C11.187.183.394 \|C11.204.564.585
Synonyms:	Keratoconjunctivitides
Slim Mappings:	Eye disease
Reference:	MedGen: D007637 MeSH: D007637 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants