SHMARQL
Docs
Query
Entity
Story editor
multiple familial trichoepithelioma
<http:/
/
www.wikidata.org/
entity/
Q928767>
human disease
rdfs:
label
ar
de
en
fr
pt
pt-br
"Brooke-Spiegler-Syndrom"
@de
"Tricoepitelioma múltiplo familiar"
@pt
"Tricoepitelioma múltiplo familiar"
@pt-br
"multiple familial trichoepithelioma"
@en
"trichoépithéliome multiple familial"
@fr
"متلازمة سي واي إل دي الجلدية"
@ar
skos:
alt
Label
"Brooke-Fordyce Trichoepitheliomas"
@en
"Epithelioma Adenoides Cysticum of Brooke"
@en
"Epithelioma, Hereditary Multiple Benign Cystic"
@en
"Mft1"
@en
"TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1"
@en
"Trichoepithelioma, Multiple Familial, type 1"
@en
schema:
description
de
en
hy
uk
"erbliche Erkrankung"
@de
"human disease"
@en
"хвороба людини"
@uk
"մարդու հիվանդություն"
@hy
schema:
date
Modified
"2026-10-24T00:39:30+00:00"
^^xsd:dateTime
schema:
version
2560167728
wikibase:
identifiers
13
wikibase:
sitelinks
3
wikibase:
statements
26
p:
P11143
wd:
statement/Q928767-4F9783D3-6613-4784-9DDB-33D51281C24B
p:
P14914
wd:
statement/Q928767-102CD7CD-2B99-451F-B990-35A2D9018466
p:
P1550
wd:
statement/Q928767-05e5fe8d-45a2-7c4d-c6df-45e972d54ef8
p:
P2293
wd:
statement/Q928767-AA72FAD5-DA30-46E7-8173-42C7F4DE11D8
p:
P279
wd:
statement/Q928767-3080B447-92E4-4973-AC09-D4C759A4DB35
wd:
statement/Q928767-62f6536f-4b3d-587b-ff98-213550a927a9
wd:
statement/Q928767-B7FE2960-249B-44E3-B84E-9FA3D0005775
wd:
statement/Q928767-f2a17603-49eb-4f63-e546-b0c6827159c8
p:
P2841
wd:
statement/Q928767-17E44E9B-0164-4700-9353-72A1C03B2FCD
p:
P2888
wd:
statement/Q928767-3E0E9073-37D0-4AAE-8046-A6D2F055DF36
wd:
statement/Q928767-7E8C2038-31D9-44D1-A727-7CD52769EE87
p:
P2892
wd:
statement/Q928767-4C5D7664-82DD-40D0-993F-E40EBA839FEB
p:
P31
wd:
statement/Q928767-3CE3EFE2-CEA5-43C1-9C96-06A97D7B72CB
wd:
statement/Q928767-BAF3622D-E1F7-43AA-86D3-04C94D81EC33
p:
P4229
wd:
statement/Q928767-7993B62C-DB1E-456F-A4AA-70E2C1E647EE
p:
P4317
wd:
statement/Q928767-C4CFE2B0-4C58-4F3A-B0EB-5E0F460369F2
p:
P486
wd:
statement/Q928767-42243b52-43a7-b37a-09ba-d302fad20bf8
p:
P492
wd:
statement/Q928767-70E7417D-DC3A-4493-B0A1-8FAAA5B6D62E
p:
P5270
wd:
statement/Q928767-0B56B747-C8D5-4F51-9CBD-893557E1DD1D
p:
P6366
wd:
statement/Q928767-4D80AEB8-BA23-48F0-94EA-F37EF9C8C59E
p:
P6532
wd:
statement/Q928767-4E1CF436-E035-4C03-8F24-97161B0619DF
wd:
statement/Q928767-CDA90ACA-1030-42AF-938B-E3FF07B92432
wd:
statement/Q928767-E06AEACF-7150-4BB3-A098-DEFC7AF2ECC3
p:
P665
wd:
statement/Q928767-39221C08-A7F0-415F-81AD-F56B88F5D834
p:
P7464
wd:
statement/Q928767-9493EB27-5B32-42E5-A444-6A5A13263B65
p:
P7807
wd:
statement/Q928767-ac273c17-41f9-4f60-f145-7a66ab57afad
p:
direct-
normalized/
P486
<http:/
/
id.nlm.nih.gov/
mesh/
C536552>
p:
direct-
normalized/
P5270
<http:/
/
purl.obolibrary.org/
obo/
MONDO_0011114>
p:
direct-
normalized/
P6366
<https:/
/
makg.org/
entity/
2779906317>
p:
direct-
normalized/
P665
<http:/
/
www.kegg.jp/
entry/
H00829>
wdt:
P11143
"CYLD cutaneous syndrome"
wdt:
P14914
"D00867"
wdt:
P1550
"867"
wdt:
P2293
CYLD
wdt:
P279
Brooke-Spiegler syndrome
trichoepithelioma
head and neck disease
wdt:
P2841
childhood onset
wdt:
P2888
<http:/
/
www.orpha.net/
ORDO/
Orphanet_79493>
<http:/
/
www.orpha.net/
ORDO/
Orphanet_867>
wdt:
P2892
"C1275122"
wdt:
P31
type of disease
rare disease
wdt:
P4229
"D23.3"
wdt:
P4317
"10867"
wdt:
P486
"C536552"
wdt:
P492
"601606"
wdt:
P5270
"MONDO_0011114"
wdt:
P6366
"2779906317"
wdt:
P6532
Telangiectasia of the skin
basal-cell carcinoma of the skin
papule
wdt:
P665
"H00829"
wdt:
P7464
"multiple-familial-trichoepithelioma"
wdt:
P7807
"480444747"
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data from SPARQL profile:
Wikidata