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LTBP2-related ocular dysgenesis

MONDO:0100236

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

0 clinical trials for this condition and its sub-types, 0 tagged with LTBP2-related ocular dysgenesis itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18187) ↑ Eye disorder (3068)

Sub-types of LTBP2-related ocular dysgenesis

Weill-Marchesani syndrome 3 0 trials
Glaucoma 3, primary congenital, D 0 trials
Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma 0 trials
1 sub-type
- Glaucoma secondary to spherophakia/ectopia lentis and megalocornea 0 trials

Including sub-types (0) Tagged with LTBP2-related ocular dysgenesis (0)

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