Anterior segment dysgenesis
MONDO:0019503A spectrum of developmental anomalies that affect the development of the anterior segment of the eyeball resulting from abnormalities of neural crest migration and differentiation during embryologic development (Axenfeld-Rieger syndrome, Peters anomaly, posterior keratoconus, and iridoschisis).
Also known as: ASGD, ASMD, ASOD, anterior segment mesenchymal dysgenesis, anterior segment ocular dysgenesis, familial ocular anterior segment mesenchymal dysgenesis
21 clinical trials for this condition and its sub-types, 2 tagged with Anterior segment dysgenesis itself.
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Sub-types of Anterior segment dysgenesis
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Congenital primary aphakia 17 trials
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Iridogoniodysgenesis 0 trials · 2 incl. sub-types
7 sub-types
- FOXC1-related anterior segment dysgenesis 0 trials · 1 incl. sub-types Sub-types →
- Congenital microcoria 1 trial
- Rieger anomaly 0 trials Sub-types →
- Aniridia-cerebellar ataxia-intellectual disability syndrome 0 trials
- Bilateral acute depigmentation of the iris 0 trials
- Chromosome 6pter-p24 deletion syndrome 0 trials
- Congenital ectropion uveae 0 trials
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Peters anomaly 1 trial
2 sub-types
- Peters anomaly-cataract syndrome 0 trials
- Von Hippel anomaly 0 trials
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Anterior segment dysgenesis 1 1 trial
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Anterior segment dysgenesis 6 1 trial
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Anterior segment dysgenesis 7 0 trials
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Anterior segment dysgenesis 8 0 trials
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Isolated iridoschisis 0 trials