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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
cataract +     
autosomal dominant cataract 
cataract 12 multiple types 
cataract 34 multiple types 
Any cataract (disease) in which the cause of the disease is a mutation in the FOXE3 gene.
cataract 49 
cataract 50 with or without glaucoma 
cortical cataract +  
diabetes mellitus type 2 associated cataract 
early-onset non-syndromic cataract +  
nuclear cataract +  
senile cataract +   

Synonyms
Exact Synonyms: CATC3 ;   CTRCT34 ;   FOXE3 cataract (disease) ;   cataract (disease) caused by mutation in FOXE3
Related Synonyms: cataract 34, multiple types, with or without microcornea ;   cataract, autosomal recessive congenital 3
Alternate IDs: MONDO:0013067
Xrefs: DOID:0110230 ;   GARD:15599 ;   MEDGEN:442822 ;   MESH:C567835 ;   MIM:612968 ;   UMLS:C2751822
Definition Sources: MONDO:patterns/disease_series_by_gene

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