Disease #05990 (KEFH (Keratoendothelitis fugax hereditaria), OMIM:148200)

Official abbreviation KEFH
Name Keratoendothelitis fugax hereditaria
OMIM ID 148200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NLRP3
Associated tissues -
Disease features -
Remarks -