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GENATLAS PHENOTYPE

last update : 10-04-2019

Symbol	ASMD5
Location	1p33
Name	ocular anterior segment mesenchymal dysgenesis 5
Corresponding gene	FOXE3
Main clinical features	heterogeneous group of developmental disorders affecting the anterior segment of the eye, including the cornea, iris, lens, trabecular meshwork, and Schlemm canal including iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface
Genetic determination	autosomal dominant
Related entries	including cataract
Function/system disorder	eye
Type	disease

Remark(s)