Preferred Label : XK aprosencephaly;
ICD-11 definition : Xk aprosencephaly represents the syndromic form of aprosencephaly and is characterized
by near total absence of the prosencephalon with a midline oculofacial defect similar
to that observed in the most severe forms of holoprosencephaly.;
Origin ID : 1805259428;
Automatic exact mappings (from CISMeF team)
Xk aprosencephaly represents the syndromic form of aprosencephaly and is characterized
by near total absence of the prosencephalon with a midline oculofacial defect similar
to that observed in the most severe forms of holoprosencephaly.
