SHMARQL

hypomyelinating leukodystrophy

<http://www.wikidata.org/entity/Q28065591>

leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system
rdfs:label
"hypomyelinating leukodystrophy"@en
skos:altLabel
"HLD"@en
schema:description
"leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system"@en
schema:dateModified "2024-02-25T22:03:10+00:00"^^xsd:dateTime
schema:version 2087225705
wikibase:identifiers 2
wikibase:sitelinks 0
wikibase:statements 8
p:P279 wd:statement/Q28065591-41936F2F-9BEE-4795-AAA5-7245ABC3D7CC
wd:statement/Q28065591-d8e5eb6b-49fa-6334-01d2-559ea946bc0c
p:P2888 wd:statement/Q28065591-4E38349C-8CF2-4CAF-B823-8C838AC56D5E
wd:statement/Q28065591-D17EE042-24CA-4838-81BB-B918879FF97C
p:P31 wd:statement/Q28065591-DEF62CDF-31F1-415D-8985-BA5761DBDC84
p:P5008 wd:statement/Q28065591-45458CCC-B44D-48C0-859A-E44415A85421
p:P665 wd:statement/Q28065591-D0BAF632-AD48-4008-96A9-DEC2B55AEABC
p:P699 wd:statement/Q28065591-448B9A87-071F-4FE6-B0BE-596429F4EEE6
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00679>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060786>
wdt:P279 Hereditary CNS demyelinating disease
leukodystrophy
wdt:P2888 <http://identifiers.org/doid/DOID:0060786>
<http://purl.obolibrary.org/obo/DOID_0060786>
wdt:P31 type of disease
wdt:P5008 WikiProject Medicine
wdt:P665 "H00679"
wdt:P699 "DOID:0060786"
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