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: |
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MeSH: |
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MedDRA: |
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Snomed: |
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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:
|
(HPO:0012040) | Corneal stromal edema | 1 / 7739 | ||||
|
(HPO:0012038) | Corneal guttata | 3 / 7739 | ||||
|
(HPO:0001131) | Corneal dystrophy | 56 / 7739 | ||||
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(HPO:0007705) | Corneal degeneration | 3 / 7739 | ||||
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(HPO:0012039) | Descemet Membrane Folds | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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