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Axenfeld anomaly

Disease Export to PDF
Name:
Axenfeld anomaly
Description:
A rare, congenital, ocular defect caused by anterior segment dysgenesis and characterized by anteriorly displaced Schwalbe's line and iris bands extending into the cornea. In contrast, Rieger's anomaly includes characteristic iris and pupil anomalies.
ORPHAcode:
98978
XREF(s):
Orphanet
OMIM
OMIM
MedDRA
ICD-10
Analyte(s):
PITX2
FOXC1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14