Duchenne muscular dystrophy

neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle
rdfs:label
"Duchenne muscular dystrophy"@en
skos:altLabel
"DMD"@en
"Duchenne-type muscular dystrophy"@en
"pseudohypertrophic progressive muscular dystrophy"@en
"severe dystrophinopathy"@en
schema:description
"neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle"@en
schema:dateModified "2026-10-30T17:08:49+00:00"^^xsd:dateTime
schema:version 2562635027
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p:direct-normalized/P227 <https://d-nb.info/gnd/4370335-5>
p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh86006749>
p:direct-normalized/P268 <http://data.bnf.fr/ark:/12148/cb12314617h#about>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D020388>
p:direct-normalized/P508 <http://purl.org/bncf/tid/55503>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010679>
p:direct-normalized/P6366 <https://makg.org/entity/2778943923>
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<http://id.nlm.nih.gov/mesh/C10.668.491.175.500.300>
<http://id.nlm.nih.gov/mesh/C16.320.322.562>
<http://id.nlm.nih.gov/mesh/C16.320.577.300>
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wdt:P10022 "distrofia-di-duchenne"
wdt:P10283 "C2778943923"
wdt:P11143 "Duchenne muscular dystrophy"
wdt:P11430 "DI-01509"
wdt:P1193 0.000159^^xsd:decimal
wdt:P12086 "Ziekte_van_Duchenne"
wdt:P1245 "710542"
wdt:P13591 "concept/42e893e7-5ffa-4e08-baf4-c3777efbc85c"
wdt:P138 Guillaume Duchenne de Boulogne
wdt:P1417 "science/Duchenne-muscular-dystrophy"
wdt:P1461 "duchenne-muscular-dystrophy"
wdt:P14914 "D98896"
wdt:P1550 "98896"
wdt:P1617 "7d4ac31f-0781-4232-a30e-0d27b47a1b23"
wdt:P1748 "C75482"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Duchenne-muscular-dystrophy.jpg>
wdt:P1995 neurology
wdt:P2176 eteplirsen
ataluren
deflazacort
wdt:P227 "4370335-5"
wdt:P2293 DMD
LTBP4
wdt:P244 "sh86006749"
wdt:P268 "12314617h"
wdt:P279 X-linked recessive disease
Duchenne and Becker muscular dystrophy
myopathy with eye involvement
wdt:P2841 childhood onset
wdt:P2888 <http://identifiers.org/doid/DOID:11723>
<http://purl.obolibrary.org/obo/DOID_11723>
<http://www.orpha.net/ORDO/Orphanet_98896>
wdt:P2892 "C0013264"
wdt:P31 type of disease
rare disease
wdt:P3417 "Duchenne-Muscular-Dystrophy"
wdt:P3471 "43506"
wdt:P373 "Duchenne muscular dystrophy"
wdt:P3827 "duchenne-muscular-dystrophy"
wdt:P4229 "G71.0"
wdt:P4233 "duchenne-dystrophy"
wdt:P4317 "6291"
wdt:P443 <http://commons.wikimedia.org/wiki/Special:FilePath/LL-Q33810%20%28ori%29-Psubhashish-%E0%AC%A1%E0%AD%81%E0%AC%B8%E0%AD%87%E0%AC%A8%20%E0%AC%AE%E0%AC%B8%E0%AD%8D%E0%AC%95%E0%AD%81%E0%AC%B2%E0%AC%BE%E0%AC%B0%20%E0%AC%A1%E0%AC%BF%E0%AC%B8%E0%AD%8D%E0%AC%9F%E0%AD%8D%E0%AC%B0%E0%AD%8B%E0%AC%AB%E0%AC%BF.wav>
wdt:P486 "D020388"
wdt:P492 "310200"
wdt:P5008 WikiProject Medicine
wdt:P508 "55503"
wdt:P5082 "Duchennes_muskeldystrofi"
wdt:P5270 "MONDO_0010679"
wdt:P557 "3985"
wdt:P604 "000705"
wdt:P6366 "2778943923"
wdt:P646 "/m/03vsh3"
wdt:P6532 motor delay
waddling gait
Delayed gross motor development
Progressive muscle weakness
Difficulty climbing stairs
contracture
skeletal muscle atrophy
obstructive sleep apnea
scoliosis
developmental language disorder
specific learning disability
global developmental delay
cognitive dysfunction
respiratory failure
cardiomyopathy
wdt:P665 "H01963"
wdt:P672 "C05.651.534.500.300"
"C10.668.491.175.500.300"
"C16.320.322.562"
"C16.320.577.300"
wdt:P691 "ph1137579"
wdt:P699 "DOID:11723"
wdt:P7293 "9810556536705606"
wdt:P7329 "8C70.1"
wdt:P780 muscle weakness
muscular atrophy
cardiomyopathy
wdt:P7807 "1479561744"
wdt:P8189 "987007529604705171"
wdt:P828 mutation
wdt:P923 magnetic resonance imaging
muscle biopsy
genetic testing
electromyography
sleep study
creatine kinase measurement
wdt:P924 physiotherapy
corticosteroid
gene therapy
occupational therapy
surgery
artificial respiration
wdt:P9322 "0433701-Duchennova-svalova-dystrofie"
wdt:P950 "XX547229"
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