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(Q55785518)
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English
rare syndrome with cardiac malformations
human disease
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default values for all languages
No label defined
No description defined
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Statements
instance of
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015506
class of disease
0 references
subclass of
rare surgical cardiac disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015506
genetic cardiac disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015506
rare genetic developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015506
Syndromes affecting the heart
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_156532
0 references
Identifiers
Mondo ID
MONDO_0015506
0 references
Orphanet ID
156532
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015506
UMLS CUI
C5680646
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
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