Disease #04336 (FECD-3 (dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)), OMIM:613267)

Official abbreviation FECD-3
Name dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)
OMIM ID 613267
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TCF4
Associated tissues -
Disease features -
Remarks -