Anterior segment dysgenesis

rare

A 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).

Identifiers: MONDO:0019503 Orphanet:88632
Part of: Disorder of development or morphogenesis Eye disorder Hereditary disease
Also known as: anterior segment mesenchymal dysgenesis · anterior segment ocular dysgenesis · ASGD · ASMD · ASOD

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Iridogoniodysgenesis	MONDO:0011119	10
Peters anomaly	MONDO:0011414	2	PAX6
Anterior segment dysgenesis 1	MONDO:0007138		PITX3
Anterior segment dysgenesis 6	MONDO:0015016
Anterior segment dysgenesis 7	MONDO:0010015		PXDN
Anterior segment dysgenesis 8	MONDO:0015017		CPAMD8
Congenital primary aphakia	MONDO:0012456		FOXE3
Isolated iridoschisis	MONDO:0033810

Rare disease

Projects

Including projects on subtypes.

No projects yet.