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: Keratitis (D007634)
..Starting node ..Keratitis Fugax Hereditaria (C563650)
Child Nodes:
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:

6043

Name:

Keratitis Fugax Hereditaria

Definition:

Alternative IDs:

ParentIDs:

MESH:D007634

TreeNumbers:

C11.204.564/C563650

Synonyms:

Keratoendotheliitis Fugax Hereditaria

Slim Mappings:

Eye disease

Reference:

MedGen: C563650
MeSH: C563650
OMIM: 148200;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0003621	Juvenile onset
3	HP:0000491	Keratitis
4	HP:0007759	Opacification of the corneal stroma

Disease Causing ClinVar Variants