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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
anterior segment dysgenesis 7 
brittle cornea syndrome 
Central cloudy dystrophy of Francois 
congenital primary aphakia 
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 
Familial amyloidosis, Finnish type 
Fuchs endothelial corneal dystrophy  
iridogoniodysgenesis +  
keratitis +  
keratoconus +   
megalocornea +  
Microcystic corneal dystrophy 
Peters anomaly +  
Peters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane.
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: Peters anomaly (disease) ;   Peters congenital glaucoma ;   anterior segment dysgenesis 5, multiple subtypes
Related Synonyms: ASGD5 ;   anterior segment dysgenesis 5
Alternate IDs: MONDO:0011414
Xrefs: DOID:0060673 ;   DOID:0080610 ;   GARD:7377 ;   HP:0000659 ;   ICD9:743.44 ;   MEDGEN:91031 ;   MESH:C537884 ;   MIM:604229 ;   MedDRA:10059202 ;   ORDO:708
Definition Sources: Orphanet:708

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