XK aprosencephaly (Q88773): Difference between revisions
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Revision as of 15:09, 15 August 2026
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 |
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| 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. |
Statements
CID11:ID_1805259428
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