Keratoendotheliitis Fugax Hereditaria (KEFH)
Alias:
Keratitis Fugax Hereditaria
Keratoendothelitis Fugax Hereditaria
Kefh
Kfh
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Keratoendotheliitis Fugax Hereditaria, also known as keratitis fugax hereditaria, is related to cryopyrin-associated periodic syndrome and keratitis, hereditary. An important gene associated with Keratoendotheliitis Fugax Hereditaria is NLRP3 (NLR Family Pyrin Domain Containing 3). Affiliated tissues include eye and skin, and related phenotypes are keratitis and opacification of the corneal stroma
Related ID:
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
1
37
3
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Sources
Back to top