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aniridia

Disease Summary
Associated Targets (7)
Tbio

5

Tchem

2


GARD Rare
Mondo Description Aniridia is a congenital ocular malformation characterized by the complete or partial absence of the iris. It can be isolated or part of a syndrome (isolated and syndromic aniridia).
Mondo Term and Equivalent IDs
MONDO:0019172:  aniridia
DOID:12271: aniridia
GARD:0005816: 
ICD9:743.45: 
MESH:D015783: 
NCIT:C84563: 
Orphanet:77: 
SCTID:69278003: 
UMLS:C0003076: