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About:
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
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An Entity of Type :
wikibase:Item
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Item
New Facet based on Instances of this Class
human disease
Attributes
Values
rdf:type
Item
description
human disease
(en)
хвороба людини
(uk)
exact match
wds:Q55787950-6B84C1EC-E411-444C-A05E-58EDF802896A
exact match
http://www.orpha.net/ORDO/Orphanet_391316
Mondo ID
wds:Q55787950-03265A68-48B7-4D35-80D2-C1A68253AAFD
Mondo ID
http://purl.obolibrary.org/obo/MONDO_0018314
Mondo ID
MONDO_0018314
rdfs:label
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
(en)
skos:prefLabel
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
(en)
name
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
(en)
instance of
wds:Q55787950-B586EFA1-33BB-4FBA-AB53-ADA1C8C24977
instance of
class of disease
subclass of
wds:Q55787950-12081210-08BE-4D68-9D46-09797927FAAD
wds:Q55787950-1FEE0C12-76AD-4B78-BE78-FA6EBAEB6633
subclass of
infancy electroclinical syndrome
monogenic disease with epilepsy
Orphanet ID
wds:Q55787950-F95BA2D0-E8B5-462D-B55C-5CE45D34EBE1
ICD-10-CM
wds:Q55787950-88F19124-91E3-49B6-8637-F41508807A2D
Orphanet ID
391316
ICD-10-CM
G40.2
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q55787950
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