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GENATLAS PHENOTYPE

last update : 13/07/2006

Symbol	IHG2
Location	4q25
Name	iridogoniodysgenesis, type 2
Other name(s)	iris hypoplasia with early onset glaucoma
Corresponding gene	PITX2
Other symbol(s)	ADIRH, IGDS, IRID2
Main clinical features	goniodysgenesis elevated intraocular pressure and secundary glaucoma (see RIEG1)
Genetic determination	autosomal dominant
Function/system disorder	eye
Type	disease

Gene product

Name	solurshin, homeo domain encoding gene (PITX2)

Remark(s)