XK aprosencephaly (Q88773): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1805259428
@@ Property / Canonical URI: https://id.who.int/icd/entity/1805259428 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1805259428
@@ Property / CURIE: CID11:ID_1805259428 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1805259428
@@ Property / Canary Token: dki-india-ID_1805259428 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest 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
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.