CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6

General Information (adopted from Orphanet):

Synonyms, Signs: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET
FECD6
Number of Symptoms 1
OrphanetNr:
OMIM Id: 613270
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001131) Corneal dystrophy 56 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Molecular genetics OMIM Riazuddin et al. (2010) analyzed the ZEB1 gene in 192 unrelated patients with adult-onset Fuchs endothelial corneal dystrophy (FECD) and identified 4 different heterozygous missense mutations in 4 patients, respectively, that were not found in 560 unrelated, ethnically ...