Disease #00461 (LCD-1 (dystrophy, corneal, lattice type I (LCD-1)), OMIM:122200)

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Official abbreviation	LCD-1
Name	dystrophy, corneal, lattice type I (LCD-1)
OMIM ID	122200
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 14:32:32 +02:00 (CEST)
Date last edited	N/A