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Ontology Browser

Term:
Central cloudy dystrophy of Francois (EFO:Orphanet:98972)
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Parent Terms Term With Siblings Child Terms
corneal disease +     
Blindness-scoliosis-arachnodactyly syndrome 
brittle cornea syndrome 
Central cloudy dystrophy of Francois 
Central cloudy dystrophy of François is a very rare form of stromal corneal dystrophy (see this term) characterized by polygonal or rounded stromal opacities surrounded by clear tissue, and generally no effect on vision.
Connective tissue disease with eye involvement +   
cornea neoplasm +  
cornea plana +  
Corneal astigmatism  
corneal degeneration +   
corneal deposit +  
corneal dystrophy +   
Corneal dystrophy - perceptive deafness 
corneal edema +   
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis 
Ectodermal malformation syndrome associated with ocular features +  
Familial amyloidosis, Finnish type 
Fuchs endothelial corneal dystrophy  
Genetic developmental defect of the eye +  
Genetic lens and zonula anomaly +  
Genetic neuro-ophthalmological disease +  
Genetic vitreous-retinal disease +  
Genodermatosis with ocular features +  
keratitis +   
keratoconus +   
megalocornea +  
Metabolic disease associated with ocular features +  
Microcystic corneal dystrophy 
Optic neuropathy +  
Peters anomaly +  
Rare disease with glaucoma as a major feature +  
Rare genetic palpebral, lacrimal system and conjunctival disease +  
Rare genetic refraction anomaly +  
Reis-Bücklers corneal dystrophy 
sclerocornea +  
Spastic ataxia - corneal dystrophy 
Subaortic stenosis - short stature 
X-linked corneal dermoid 
X-linked reticulate pigmentary disorder with systemic manifestations 

Synonyms
Exact Synonyms: CCDF ;   Central cloudy corneal dystrophy of Francois
Xrefs: ICD10:H18.5 ;   MIM:217600 ;   UMLS:C1622427

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