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(Q55788337)
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English
genetic cerebral small vessel disease
human disease
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default values for all languages
No label defined
No description defined
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Statements
instance of
class of disease
0 references
subclass of
genetic central nervous system and retinal vascular disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018787
central nervous system and retinal vascular disease
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018787
exact match
http://www.orpha.net/ORDO/Orphanet_477754
0 references
Identifiers
ICD-11 ID (Foundation)
133909731
0 references
ICD-11 ID (MMS)
8B22.C
subject named as
Hereditary cerebrovascular diseases
0 references
Mondo ID
MONDO_0018787
0 references
Orphanet ID
477754
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0018787
UMLS CUI
C5681259
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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