dilated cardiomyopathy 1R

dilated cardiomyopathy that has material basis in mutation in the ACTC1 gene on chromosome 15q14
rdfs:label "dilated cardiomyopathy 1R"@en
skos:altLabel "CARDIOMYOPATHY, DILATED, 1R"@en
"CARDIOMYOPATHY, DILATED, 1R; CMD1R"@en
"CMD1R"@en
"Cardiomyopathy, Dilated, type 1R"@en
"Left Ventricular Noncompaction 4"@en
"dilated cardiomyopathy type 1R"@en
schema:description
"dilated cardiomyopathy that has material basis in mutation in the ACTC1 gene on chromosome 15q14"@en
schema:dateModified "2025-07-20T19:24:38+00:00"^^xsd:dateTime
schema:version 2382094996
wikibase:identifiers 7
wikibase:sitelinks 0
wikibase:statements 16
p:P11430 wd:statement/Q28024581-cabac312-4ae2-25eb-a245-65510813984d
p:P1995 wd:statement/Q28024581-DAEFEDBC-3B0D-49AD-8FF9-AB8A7732FA67
p:P2293 wd:statement/Q28024581-3B77FDAB-8404-4C4B-BD95-D6EF768F740D
p:P279 wd:statement/Q28024581-1ADAA2FA-1FD4-4B3F-83FC-62D4A5B220E9
wd:statement/Q28024581-A4C749AD-A8D5-4F8D-8C21-FDE8B7A65886
p:P2888 wd:statement/Q28024581-19880D1B-AE70-4842-9213-FC7A95C135A5
wd:statement/Q28024581-E4E63910-865C-4961-A4DB-B3B19CE22C54
p:P2892 wd:statement/Q28024581-2EE08F60-FFB5-4565-859C-FF4B4E19C2A5
wd:statement/Q28024581-8F142FF6-BA5F-465E-AC25-2D17FDD9F3BA
p:P31 wd:statement/Q28024581-108DE6A0-94B8-4F4D-A6C2-FD2643D061F0
wd:statement/Q28024581-23C1DFB8-6E7B-44BA-B3FD-09FA92BADDDB
p:P4229 wd:statement/Q28024581-19312DC7-0069-49BE-A803-766436F28210
p:P492 wd:statement/Q28024581-7408CCBC-6AEB-42FE-B365-CACAAD070DF7
p:P5008 wd:statement/Q28024581-8CE7D87E-665A-450E-BCD9-2C5FB5ED82B3
p:P5270 wd:statement/Q28024581-58CC3231-6F5F-4011-902F-37554F3A67CB
p:P699 wd:statement/Q28024581-29E7F351-2145-43B7-B6AF-A748351F67E8
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0013261>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110456>
wdt:P11430 "DI-00223"
wdt:P1995 cardiology
wdt:P2293 ACTC1
wdt:P279 genetic disease
dilated cardiomyopathy
wdt:P2888 <http://identifiers.org/doid/DOID:0110456>
<http://purl.obolibrary.org/obo/DOID_0110456>
wdt:P2892 "C3150681"
"C3150682"
wdt:P31 type of disease
rare disease
wdt:P4229 "I42.0"
wdt:P492 "613424"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0013261"
wdt:P699 "DOID:0110456"
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