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Details for Disease 782

DISEASE NAME	Axenfeld-Rieger syndrome
DISEASE CATEGORY (ICD10)	Congenital malformations, deformations and chromosomal abnormalities
DISEASE ID (ICD10)	Q13.8
DISEASE ID (OMIM)	180500; 601499; 602482
1 combination linked to 782	OLI253
1 gene combination linked to 782	FOXC1; PITX2
ORPHANET ID	782

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