Duchenne muscular dystrophy (Q41380): Difference between revisions

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+https://id.who.int/icd/entity/1479561744
@@ Property / Canonical URI: https://id.who.int/icd/entity/1479561744 / rank @@
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@@ Property / CURIE @@
+CID11:8C70.1
@@ Property / CURIE: CID11:8C70.1 / rank @@
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+dki-india-8C70.1
@@ Property / Canary Token: dki-india-8C70.1 / rank @@
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+August 2026Timestamp +2026-08-13T00:00:00Z
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Calendar Gregorian
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+G71.0
@@ Property / Linked ICD 10: G71.0 / rank @@
+Normal rank

Latest revision as of 07:31, 13 August 2026

Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking.

Language	Label	Description	Also known as
default for all languages	8C70.1
English	Duchenne muscular dystrophy	Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking.