LTBP2-related ocular dysgenesis

Any ocular dysgenesis disorder in which the cause of the disease is a mutation in the LTBP2 gene.

Subtypes

Disease	ID	Subtypes
Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma	MONDO:0009633	1
Weill-Marchesani syndrome 3	MONDO:0013899
Glaucoma 3, primary congenital, D	MONDO:0013122

Rare disease

Including projects on subtypes.

No projects yet.