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(Q6172449)
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English
Jeavons syndrome
Type of epilepsy
EMEA
Eyelid myoclonia with and without absences
epilepsy with eyelid myoclonias
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No label defined
No description defined
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Statements
instance of
Idiopathic generalized epilepsy
0 references
class of disease
0 references
subclass of
Epilepsy in children
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015346
generalized epilepsy
0 references
exact match
http://www.orpha.net/ORDO/Orphanet_139431
0 references
Identifiers
ICD-10-CM
G40.3
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015346
ICD-11 ID (Foundation)
262814036
0 references
Microsoft Academic ID
2780325231
0 references
2910578444
0 references
Mondo ID
MONDO_0015346
0 references
Orphanet ID
139431
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0015346
UMLS CUI
C4274731
0 references
Sitelinks
Wikipedia
(3 entries)
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arwiki
متلازمة جيفزنز
enwiki
Jeavons syndrome
hewiki
תסמונת ג'ייוונס
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Wikiversity
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Wikivoyage
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