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rdfs:label
|
"autoimmune lymphoproliferative syndrome type 2A"@en
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|
skos:altLabel
|
"ALPS-CASP10"@en
|
|
"ALPS2A"@en
|
|
"AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA"@en
|
|
"AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA; ALPS2A"@en
|
|
"Autoimmune Lymphoproliferative Syndrome, Type 2"@en
|
|
"Autoimmune Lymphoproliferative Syndrome-CASP10 variant"@en
|
|
"Type 2 ALPS"@en
|
|
"Type 2 Autoimmune Lymphoproliferative Syndrome"@en
|
|
"autoimmune lymphoproliferative syndrome type IIA"@en
|
|
schema:description
|
"Krankheit"@de
"autoimmune lymphoproliferative syndrome that has material basis in mutation in the CASP10 gene"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T12:32:50+00:00"^^xsd:dateTime
|
|
schema:version
|
2514121311
|
|
wikibase:identifiers
|
9
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
19
|
|
p:P11430
|
wd:statement/Q27677633-8935dc66-4930-bc3b-92c6-ba8f5d793ffa
|
|
p:P1748
|
wd:statement/Q27677633-3D342056-D891-490B-B3EC-D215835DBAF4
|
|
p:P2293
|
wd:statement/Q27677633-9C19C062-BF5C-40EA-8C44-C74C41208320
|
|
p:P279
|
wd:statement/Q27677633-26C9B691-2DEC-488E-AE22-6B2A0E2A7D7C
|
|
wd:statement/Q27677633-291e52b1-4ba9-da30-eaec-f649038a8c76
|
|
wd:statement/Q27677633-62CFFF6F-401B-4102-8355-C5840CF854EB
|
|
p:P2888
|
wd:statement/Q27677633-392D4CE5-7420-4ABF-BF21-6F77F3005072
|
|
wd:statement/Q27677633-AC8489C1-C74E-4247-89BE-682C130684B8
|
|
p:P2892
|
wd:statement/Q27677633-0027B86E-CD0D-47B7-97BD-A03937BBCBBB
|
|
wd:statement/Q27677633-56283C70-AB86-4DB9-84BC-27816DC571FD
|
|
p:P31
|
wd:statement/Q27677633-57E81DB9-2824-4770-892D-52D67359FBDB
|
|
wd:statement/Q27677633-CB318FA9-55A2-4321-9706-6B6DA5F948DC
|
|
p:P4229
|
wd:statement/Q27677633-E8B43E47-4F77-42AE-B500-F08ED23085DE
|
|
p:P486
|
wd:statement/Q27677633-4EC64D82-625D-4DD2-B539-94D40A9A48D1
|
|
p:P492
|
wd:statement/Q27677633-06D4D6E0-238E-49C7-8E0F-5E0DBEE302F8
|
|
p:P5008
|
wd:statement/Q27677633-FE5D539E-B251-434D-A7AE-B36D091CD647
|
|
p:P5270
|
wd:statement/Q27677633-8D3552A2-657D-47ED-AF85-6F84C1156D24
|
|
p:P699
|
wd:statement/Q27677633-D1AE5474-7D8F-4251-9977-399113F5E4DA
|
|
p:P7807
|
wd:statement/Q27677633-5365b63e-4348-ff2c-de9b-1b2c9f594e61
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C565833>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0011383>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110115>
|
|
wdt:P11430
|
"DI-00157"
|
|
wdt:P1748
|
"C39576"
|
|
wdt:P2293
|
CASP10
|
|
wdt:P279
|
autosomal dominant disease
|
|
Type 2 Autoimmune Lymphoproliferative Syndrome
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110115>
|
|
<http://purl.obolibrary.org/obo/DOID_0110115>
|
|
wdt:P2892
|
"C1519709"
|
|
"C1858968"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"D47.9"
|
|
wdt:P486
|
"C565833"
|
|
wdt:P492
|
"603909"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0011383"
|
|
wdt:P699
|
"DOID:0110115"
|
|
wdt:P7807
|
"888560997"
|