Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 02-04-2019

Symbol	AIC2
Location	11p15.3
Name	Aicardi syndrome 2
Corresponding gene	TEAD1
Main clinical features	congenital neurodevelopmental disorder characterized by infantile spasms, agenesis of the corpus callosum, and chorioretinal lacunae
Genetic determination	not applicable
Function/system disorder	neurology
	eye
Type	disease

Remark(s)