Congenital muscular dystrophy type 1B (Q103686): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/222998722
@@ Property / Canonical URI: https://id.who.int/icd/entity/222998722 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_222998722
@@ Property / CURIE: CID11:ID_222998722 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_222998722
@@ Property / Canary Token: dki-india-ID_222998722 / 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 09:26, 17 August 2026

Congenital Muscular Dystrophy Type 1B is a congenital muscular disorder characterised by muscle hypotonia, weakness of proximal muscles, hypertrophy of some muscles, rigidity of the spine, and muscle contractures especially of the Achilles tendon. This form has been linked to an as yet unidentified gene on chromosome 1 and is classified as a subtype of the dystroglycanopathies.

Language	Label	Description	Also known as
default for all languages	ID_222998722
English	Congenital muscular dystrophy type 1B	Congenital Muscular Dystrophy Type 1B is a congenital muscular disorder characterised by muscle hypotonia, weakness of proximal muscles, hypertrophy of some muscles, rigidity of the spine, and muscle contractures especially of the Achilles tendon. This form has been linked to an as yet unidentified gene on chromosome 1 and is classified as a subtype of the dystroglycanopathies.