dilated cardiomyopathy 1BB

dilated cardiomyopathy that has material basis in mutation the DSG2 gene on chromosome 18q12.1
rdfs:label "dilated cardiomyopathy 1BB"@en
skos:altLabel "CARDIOMYOPATHY, DILATED, 1BB"@en
"CARDIOMYOPATHY, DILATED, 1BB; CMD1BB"@en
"CMD1BB"@en
"Cardiomyopathy, Dilated, type 1Bb"@en
"dilated cardiomyopathy type 1BB"@en
schema:description
"dilated cardiomyopathy that has material basis in mutation the DSG2 gene on chromosome 18q12.1"@en
schema:dateModified "2026-07-05T11:13:33+00:00"^^xsd:dateTime
schema:version 2514104519
wikibase:identifiers 7
wikibase:sitelinks 0
wikibase:statements 17
p:P11430 wd:statement/Q28024583-fd90c6c6-44a1-149d-543f-6ab4355c8329
p:P1995 wd:statement/Q28024583-FAF48CE8-D1D3-4F89-AFA4-918F3148633F
p:P2293 wd:statement/Q28024583-1D4CC3DF-AB9B-4168-98E4-41129F61DE86
p:P279 wd:statement/Q28024583-39B85942-A081-4C05-BCB5-9614E65B23FD
wd:statement/Q28024583-3D2E806B-D263-4184-B60E-62D61EE1FC52
wd:statement/Q28024583-7BB6F91E-00F7-4169-AE81-A3CCAE0E886C
p:P2888 wd:statement/Q28024583-596B348F-FCE5-4A28-938E-FF0A381DFDA2
wd:statement/Q28024583-C5DFEB47-AA04-4487-9F40-9F4AC7B24995
p:P2892 wd:statement/Q28024583-3C64DD9F-C574-41E0-BE10-563FB109DDFA
p:P31 wd:statement/Q28024583-31524779-6681-4841-B648-189247EEAFD7
wd:statement/Q28024583-3865BCE7-BB81-45F0-871B-AC5ED863F714
p:P4229 wd:statement/Q28024583-BB189917-6982-495F-A3E5-817A8010A355
p:P486 wd:statement/Q28024583-A3F70828-F3F8-4B41-98AC-BD60E5C9ACD3
p:P492 wd:statement/Q28024583-092EE5D3-8298-4BB3-A1AA-94B9572C964C
p:P5008 wd:statement/Q28024583-A25B0A86-AA5B-431D-9414-661AF0E7DC78
p:P5270 wd:statement/Q28024583-8A3DAA27-0AFB-418B-A1E2-2DE61C784A90
p:P699 wd:statement/Q28024583-02C552C8-DAE1-4553-AF4C-0D32EA5E076C
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C567877>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0013030>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110458>
wdt:P11430 "DI-02483"
wdt:P1995 cardiology
wdt:P2293 DSG2
wdt:P279 monogenic disease
dilated cardiomyopathy
wdt:P2888 <http://identifiers.org/doid/DOID:0110458>
<http://purl.obolibrary.org/obo/DOID_0110458>
wdt:P2892 "C2752072"
wdt:P31 type of disease
rare disease
wdt:P4229 "I42.0"
wdt:P486 "C567877"
wdt:P492 "612877"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0013030"
wdt:P699 "DOID:0110458"
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