XK aprosencephaly (Q88773)

XK aprosencephaly represents the syndromic form of aprosencephaly and is characterised by near total absence of the prosencephalon with a midline oculofacial defect similar to that observed in the most severe forms of holoprosencephaly.

Language	Label	Description	Also known as
default for all languages	ID_1805259428
English	XK aprosencephaly	XK aprosencephaly represents the syndromic form of aprosencephaly and is characterised by near total absence of the prosencephalon with a midline oculofacial defect similar to that observed in the most severe forms of holoprosencephaly.