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English
dilated cardiomyopathy 1DD
dilated cardiomyopathy that has material basis in mutation in the RBM20 gene on chromosome 10q25
CMD1DD
CARDIOMYOPATHY, DILATED, 1DD
dilated cardiomyopathy type 1DD
CARDIOMYOPATHY, DILATED, 1DD; CMD1DD
Cardiomyopathy, Dilated, type 1Dd
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
dilated cardiomyopathy
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0110447
genetic disease
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0110447
health specialty
cardiology
0 references
genetic association
RBM20
2 references
stated in
UniProt
UniProt protein ID
Q5T481
retrieved
13 August 2019
stated in
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy
on focus list of Wikimedia project
WikiProject Medicine
0 references
NCI Thesaurus ID
C174435
mapping relation type
exact match
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0110447
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110447
http://identifiers.org/doid/DOID:0110447
1 reference
stated in
Identifiers.org
reference URL
http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
Identifiers
MeSH descriptor ID
C567725
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013168
Disease Ontology ID
DOID:0110447
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110447
ICD-10-CM
I42.0
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110447
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013168
Mondo ID
MONDO_0013168
0 references
OMIM ID
613172
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110447
UMLS CUI
C2750995
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013168
UniProt disease ID
DI-02568
0 references
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Wikiversity
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Wiktionary
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