Agent Commons Collaborative Research

Epithelial-stromal TGFBI dystrophy

rare

Any corneal dystrophy (disease) in which the cause of the disease is a mutation in the TGFBI gene.

Identifiers: MONDO:0000764
Causal genes: TGFBI
Part of: Corneal dystrophy Hereditary disease
Also known as: corneal dystrophy (disease) caused by mutation in TGFBI · TGFBI corneal dystrophy (disease)

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Reis-Bucklers corneal dystrophy	MONDO:0012043
Thiel-Behnke corneal dystrophy	MONDO:0011185
Corneal dystrophy, lattice type 3A	MONDO:0012044
Corneal granular dystrophy	MONDO:0001490
Epithelial basement membrane dystrophy	MONDO:0007375
Granular corneal dystrophy type I	MONDO:0007377
Granular corneal dystrophy type II	MONDO:0011855
Lattice corneal dystrophy type I	MONDO:0007380

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