Charcot-Marie-Tooth disease type 4H (Q104658): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A doença de Charcot-Marie-Tooth tipo 4H (CMT4H) é uma polineuropatia periférica sensitivomotora da CMT desmielinizante com início nos primeiros dois anos de vida com fraqueza muscular lentamente progressiva nas extremidades distais.
@@ description / en / description / en @@
+Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy with onset within the first two years of life with slowly progressive muscle weakness in the distal extremities.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/214411126
@@ Property / Canonical URI: https://id.who.int/icd/entity/214411126 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_214411126
@@ Property / CURIE: CID11:ID_214411126 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_214411126
@@ Property / Canary Token: dki-india-ID_214411126 / 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 +2026-08-16T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-16T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 16 August 2026 / rank @@
+Normal rank

Latest revision as of 10:31, 17 August 2026

Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy with onset within the first two years of life with slowly progressive muscle weakness in the distal extremities.

Language	Label	Description	Also known as
default for all languages	ID_214411126
English	Charcot-Marie-Tooth disease type 4H	Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy with onset within the first two years of life with slowly progressive muscle weakness in the distal extremities.