Fuchs endothelial corneal dystrophy

General Information (adopted from Orphanet):

Synonyms, Signs: FECD
Late hereditary endothelial dystrophy
Endoepithelial corneal dystrophy
Number of Symptoms 6
OrphanetNr: 98974
OMIM Id: 136800
610158
613267
613268
613269
613270
613271
615523
ICD-10: H18.5
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
Multifactorial
Not applicable
[Orphanet]
Age of onset: Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Posterior corneal dystrophy
 -Rare eye disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
(HPO:0012040) Corneal stromal edema 1 / 7739
2
(HPO:0012038) Corneal guttata 3 / 7739
3
(HPO:0001131) Corneal dystrophy 56 / 7739
4
(HPO:0007705) Corneal degeneration 3 / 7739
5
(HPO:0012039) Descemet Membrane Folds 1 / 7739
6
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: