Pontocerebellar hypoplasia type 1 (Q90419): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Hipoplasia pontocerebelar tipo I é um transtorno congênito letal de morfogênese cerebral; características clínicas incluem contraturas congênitas, insuficiência respiratória, disfunção motora central e periférica e degeneração do corno anterior espinal.
@@ description / en / description / en @@
+Pontocerebellar hypoplasia type I is a lethal congenital disorder of brain morphogenesis; clinical features include congenital contractures, respiratory insufficiency, central and peripheral motor dysfunction and spinal anterior horn degeneration.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1227773923
@@ Property / Canonical URI: https://id.who.int/icd/entity/1227773923 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1227773923
@@ Property / CURIE: CID11:ID_1227773923 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1227773923
@@ Property / Canary Token: dki-india-ID_1227773923 / 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 17:23, 15 August 2026

Pontocerebellar hypoplasia type I is a lethal congenital disorder of brain morphogenesis; clinical features include congenital contractures, respiratory insufficiency, central and peripheral motor dysfunction and spinal anterior horn degeneration.

Language	Label	Description	Also known as
default for all languages	ID_1227773923
English	Pontocerebellar hypoplasia type 1	Pontocerebellar hypoplasia type I is a lethal congenital disorder of brain morphogenesis; clinical features include congenital contractures, respiratory insufficiency, central and peripheral motor dysfunction and spinal anterior horn degeneration.