dilated cardiomyopathy 1I

dilated cardiomyopathy that has material basis in mutation in the DES gene on chromosome 2q35
rdfs:label "dilated cardiomyopathy 1I"@en
skos:altLabel "CARDIOMYOPATHY, DILATED, 1I"@en
"CARDIOMYOPATHY, DILATED, 1I; CMD1I"@en
"CMD1I"@en
"Cardiomyopathy, Dilated, type 1I"@en
"dilated cardiomyopathy type 1I"@en
schema:description
"dilated cardiomyopathy that has material basis in mutation in the DES gene on chromosome 2q35"@en
schema:dateModified "2026-07-05T11:13:38+00:00"^^xsd:dateTime
schema:version 2514104549
wikibase:identifiers 7
wikibase:sitelinks 0
wikibase:statements 17
p:P11430 wd:statement/Q28024554-0dc2b1f9-4a68-391d-69ee-6de812a87682
p:P1995 wd:statement/Q28024554-C4059B1F-4F39-4645-BCE9-A4A08D0D464D
p:P2293 wd:statement/Q28024554-D46C2047-D327-43B2-95A6-3CD98C720A2C
p:P279 wd:statement/Q28024554-0918BCDE-0CCD-4441-BB5A-B0914FEFA047
wd:statement/Q28024554-77A38ACA-BA84-4366-B5A6-0E20F3982318
wd:statement/Q28024554-DDFE99C9-44BE-4D7F-A5DA-789519CB7719
p:P2888 wd:statement/Q28024554-449C986A-4764-4169-8284-7716DAC26DDC
wd:statement/Q28024554-47D56250-651F-4FC4-B864-DF5764FF9598
p:P2892 wd:statement/Q28024554-E1843626-3C1E-44A0-804D-65E69C9E9F6F
p:P31 wd:statement/Q28024554-C7CB1E59-9358-4A8C-B2DA-B376478618C8
wd:statement/Q28024554-F4DB66F5-ADBC-4592-BBDC-32C0FC2EBFD3
p:P4229 wd:statement/Q28024554-FD4C7351-4577-4E51-B1A1-243E69072904
p:P486 wd:statement/Q28024554-3DB8BFF7-7774-4FF3-89BB-692270BC7AF3
p:P492 wd:statement/Q28024554-EE1F977D-522B-47D9-96D1-7C221905F9B7
p:P5008 wd:statement/Q28024554-D3ACCCDE-8671-49CF-BBE6-067FDA898434
p:P5270 wd:statement/Q28024554-AF62B4CE-3F3E-45B6-81B1-BBDAD19DEAB7
p:P699 wd:statement/Q28024554-CEA896C8-F618-4945-8771-587F589CA117
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C565752>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0011482>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110431>
wdt:P11430 "DI-00216"
wdt:P1995 cardiology
wdt:P2293 DES
wdt:P279 monogenic disease
dilated cardiomyopathy
wdt:P2888 <http://identifiers.org/doid/DOID:0110431>
<http://purl.obolibrary.org/obo/DOID_0110431>
wdt:P2892 "C1858154"
wdt:P31 type of disease
rare disease
wdt:P4229 "I42.0"
wdt:P486 "C565752"
wdt:P492 "604765"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0011482"
wdt:P699 "DOID:0110431"
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