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A reference for what the literature reports. Not medical advice.

Disease

LTBP2-related ocular dysgenesis

MONDO:0100236Mondo

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Findings

No curated finding names LTBP2-related ocular dysgenesis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

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

Definition from the Mondo Disease Ontology (MONDO:0100236), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: eye disorder
hereditary disease
Narrower terms (3): glaucoma 3, primary congenital, D
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma
Weill-Marchesani syndrome 3