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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
corneal dystrophy +     
autosomal dominant keratitis 
Chandler syndrome 
corneal dystrophy, punctiform and polychromatic pre-descemet 
corneal endothelial dystrophy +   
epithelial and subepithelial corneal dystrophy +  
epithelial-stromal TGFBI dystrophy +  
Finnish type amyloidosis 
posterior corneal dystrophy +   
Posterior corneal dystrophies refers to a group of rare genetically determined corneal dystrophies (CDs) characterized by lesions affecting the corneal endothelium and Descemet membrane, and variable effects on vision depending on the type of dystrophy.
stromal corneal dystrophy +  
superficial corneal dystrophy +  

Synonyms
Alternate IDs: MONDO:0020214
Xrefs: GARD:19520 ;   ICD9:371.58 ;   MEDGEN:810969 ;   ORDO:98627 ;   SCTID:35091000119101 ;   UMLS:C2063478 ;   icd11.foundation:570101963
External Ontologys: disease_has_location EFO:UBERON:0004367
Definition Sources: Orphanet:98627

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