SHMARQL
Docs
Query
Entity
Story editor
central congenital hypothyroidism
<http:/
/
www.wikidata.org/
entity/
Q55786205>
rdfs:
label
en
fr
pt
pt-br
"Hipotireoidismo central"
@pt
"Hipotireoidismo central"
@pt-br
"central congenital hypothyroidism"
@en
"hypothyroïdie congénitale centrale"
@fr
skos:
alt
Label
"Central Hypothyroidism"
@en
"Hypothalamic-Pituitary Hypothyroidism"
@en
"Secondary hypothyroidism"
@en
"Thyroid Stimulating Hormone Deficiency"
@en
"Thyrotropin Deficiency"
@en
schema:
date
Modified
"2026-10-23T23:41:31+00:00"
^^xsd:dateTime
schema:
version
2560157384
wikibase:
identifiers
11
7
wikibase:
sitelinks
0
wikibase:
statements
23
p:
P14914
wd:
statement/Q55786205-7DA199B4-CA16-4833-9A65-B15D6AEF8945
p:
P1550
wd:
statement/Q55786205-024FB8BE-5FE7-47CD-922C-FF6208CF2F15
p:
P1748
wd:
statement/Q55786205-C1AFE379-6FB3-430A-8E27-1DEA9F6F9B11
p:
P2293
wd:
statement/Q55786205-468B51D2-0AC5-42C4-B6DE-37DA2ABC3FDA
wd:
statement/Q55786205-59E17F47-58C0-4B8E-AE7A-771CC3CA2D53
wd:
statement/Q55786205-5C3C066B-09BC-4D6C-90D3-F18B4521D327
wd:
statement/Q55786205-5EBDA27E-C6D9-437A-B231-9CB82C9CD652
wd:
statement/Q55786205-71125CFD-CDBD-4865-84B6-D4252754A4B9
wd:
statement/Q55786205-A9744C10-74EE-4923-8A12-F8F9B58F0185
wd:
statement/Q55786205-B2EB681E-9AE6-4600-A5A3-E88D6FC04F81
wd:
statement/Q55786205-C507B6E5-F990-4177-9560-A4837A16058A
wd:
statement/Q55786205-D5991F3E-ABD4-4DED-9269-61BEE53B7786
p:
P279
wd:
statement/Q55786205-82BB20CC-1BA9-4CCF-AFC7-7627BEEF516D
p:
P2888
wd:
statement/Q55786205-3140C272-A853-4E7E-93E0-4F2E8B5F9A70
p:
P2892
wd:
statement/Q55786205-212BD539-EA3D-43D7-952B-E9818515CB2D
wd:
statement/Q55786205-CFD5BC31-F970-4BF2-A0B0-323960C6FF26
p:
P31
wd:
statement/Q55786205-462670F2-4E54-40F0-AC19-8C4D58E6DF46
p:
P3841
wd:
statement/Q55786205-157F0082-287E-4956-8F0B-D712989C4DDC
wd:
statement/Q55786205-27BEB254-3FB7-4A62-BCF0-23B10680989D
p:
P4229
wd:
statement/Q55786205-1F4D8B81-855E-4F3A-8DB2-0E2A61C209DC
p:
P4233
wd:
statement/Q55786205-558aab06-463d-bb30-e74a-3ca0f4b94e90
p:
P4317
wd:
statement/Q55786205-FF67A49C-4836-46D3-BE35-71A1D51FBA62
p:
P5270
wd:
statement/Q55786205-62068A3F-11C2-4FB8-93EB-0D340652D2BA
p:
direct-
normalized/
P5270
<http:/
/
purl.obolibrary.org/
obo/
MONDO_0016410>
wdt:
P14914
"D226298"
wdt:
P1550
"226298"
wdt:
P1748
"C113144"
wdt:
P2293
TRHR
POU1F1
HESX1
IGSF1
PROP1
TRH
TSHB
LHX3
LHX4
wdt:
P279
permanent congenital hypothyroidism
wdt:
P2888
<http:/
/
www.orpha.net/
ORDO/
Orphanet_226298>
wdt:
P2892
"C0271801"
"C3665349"
wdt:
P31
type of disease
wdt:
P3841
"HP:0008245"
"HP:0011787"
wdt:
P4229
"E03.1"
wdt:
P4233
"central-hypothyroidism"
wdt:
P4317
"12280"
wdt:
P5270
"MONDO_0016410"
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data from SPARQL profile:
Wikidata