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Epithelial-stromal TGFBI dystrophy

MONDO:0000764

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

Also known as: TGFBI corneal dystrophy (disease), corneal dystrophy (disease) caused by mutation in TGFBI

17 clinical trials for this condition and its sub-types.

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Sub-types

Epithelial basement membrane dystrophy (1) Corneal dystrophy, lattice type 3A (0) Corneal granular dystrophy (0) Granular corneal dystrophy type I (0) Granular corneal dystrophy type II (0) Lattice corneal dystrophy type I (0) Reis-Bucklers corneal dystrophy (0) Thiel-Behnke corneal dystrophy (0)

Broader categories

Disease (618) Hereditary disease (172) Eye disorder (97) Corneal disorder (39) Human disease (14) Corneal dystrophy (4) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Disease by body system or component (0)
Trials to join now! 12 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2 Terminated 1
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