Disease #00462 (CDA (dystrophy, cornea, Avellino type (CDA)), OMIM:607541)

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Official abbreviation	CDA
Name	dystrophy, cornea, Avellino type (CDA)
OMIM ID	607541
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TGFBI
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-21 14:34:39 +02:00 (CEST)
Date last edited	N/A