Syndromes with holoprosencephaly as a major feature (Q49819): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1723390898
@@ Property / Canonical URI: https://id.who.int/icd/entity/1723390898 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD20.3
@@ Property / CURIE: CID11:LD20.3 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD20.3
@@ Property / Canary Token: dki-india-LD20.3 / 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
@@ Property / Linked ICD 10 @@
+XVII
@@ Property / Linked ICD 10: XVII / rank @@
+Normal rank

Latest revision as of 20:18, 13 August 2026

Any syndrome caused by failure of the prosencephalon to divide in two during the antenatal period. These syndromes may present with closely spaced eyes, cyclopia, flat nasal bridge, single maxillary central incisor, small head size, and clefts of the lip and palate.

Language	Label	Description	Also known as
default for all languages	LD20.3
English	Syndromes with holoprosencephaly as a major feature	Any syndrome caused by failure of the prosencephalon to divide in two during the antenatal period. These syndromes may present with closely spaced eyes, cyclopia, flat nasal bridge, single maxillary central incisor, small head size, and clefts of the lip and palate.