Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 27/09/2005

Symbol	HPEL1
Location	3p21.31
Name	holoprosencephaly-like syndrome
Corresponding gene	TDGF1
Main clinical features	severe midline brain anomalies, absence of septum pellucidum, hypoplasia of the corpus callosum and optic nerves and chiasma
Genetic determination
Function/system disorder	congenital malformation
	neurology
Type	disease

Gene product

Name	tetracarcinoma-derived growth factor 1

Remark(s)