Disease #00465 (CDL-3A (dystrophy, corneal, lattice type IIIA (CDL-3A)), OMIM:608471)

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Official abbreviation	CDL-3A
Name	dystrophy, corneal, lattice type IIIA (CDL-3A)
OMIM ID	608471
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 14:41:21 +02:00 (CEST)
Date last edited	N/A