Disease #02487 (Peters (Peters anomaly), OMIM:604229)

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Official abbreviation	Peters
Name	Peters anomaly
OMIM ID	604229
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	CYP1B1, PAX6, PITX2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A