Central cloudy dystrophy of Francois
General Information (adopted from Orphanet):
| Synonyms, Signs: |
CORNEAL DYSTROPHY, CENTRAL TYPE CCDF Central cloudy corneal dystrophy of Francois |
| Number of Symptoms | 3 |
| OrphanetNr: | 98972 |
| OMIM Id: |
217600
|
| 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 [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Posterior corneal dystrophy
-Rare eye disease -Rare genetic disease |
Symptom Information:
|
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(HPO:0007881) | Central corneal dystrophy | 1 / 7739 | ||||
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(HPO:0001131) | Corneal dystrophy | 56 / 7739 | ||||
|
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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