SHMARQL

hereditary haemochromatosis

<http://www.wikidata.org/entity/Q3144934>

metal metabolism disorder characterized by the accumulation of iron in various organs of the body
rdfs:label
"hereditary haemochromatosis"@en
skos:altLabel
"Celtic curse"@en
"HFE hereditary hemochromatosis"@en
"Haemochromatosis"@en
"Hemochromatosis, Hereditary"@en
"diabetes bronze"@en
"hemochromatosis"@en
"iron storage disorder"@en
schema:description
"metal metabolism disorder characterized by the accumulation of iron in various organs of the body"@en
schema:dateModified "2026-08-03T01:46:58+00:00"^^xsd:dateTime
schema:version 2526566052
wikibase:identifiers 30
wikibase:sitelinks 17
wikibase:statements 49
p:P10283 wd:statement/Q3144934-5A1874DC-D81B-4EA8-A1B6-BB24E2D00309
p:P11143 wd:statement/Q3144934-137F10F6-05A9-4275-B901-89DB9CFB6531
p:P11956 wd:statement/Q3144934-35099E23-4FEB-4EB1-AA7E-153E8B233E77
p:P1299 wd:statement/Q3144934-9364706B-39FF-47DB-8BAF-67B35C574FA8
p:P13204 wd:statement/Q3144934-4C6D4770-C32C-4CDA-A22C-FAAAFC7C7430
p:P1417 wd:statement/Q3144934-9086B9C3-0759-458B-9145-BB7CB97D6A16
p:P1542 wd:statement/Q3144934-8e7a2f42-41a6-54a4-f81d-59fc9da6f115
p:P1550 wd:statement/Q3144934-1F2DA856-3744-455F-A51D-AD2DDEB2AE53
wd:statement/Q3144934-E04762AA-93ED-43CA-B536-C8D345C74DDE
p:P1748 wd:statement/Q3144934-0447F76F-181C-44AA-A8EC-9B891B7FB7AB
p:P1995 wd:statement/Q3144934-4E1145A7-DE88-41D5-A910-9F320690FDE8
wd:statement/Q3144934-dd207386-4d74-33a1-a390-b51d3b239da5
p:P2176 wd:statement/Q3144934-2C474AAC-5DF1-47F5-BA6E-5F4109837EAD
wd:statement/Q3144934-3200E1DA-5724-4A67-AC43-69F2009E55F6
wd:statement/Q3144934-8E61BB3B-C286-4E53-81E7-566AF51BC88F
p:P2293 wd:statement/Q3144934-DD118DC9-0393-4598-940D-8FE4480C6F58
p:P279 wd:statement/Q3144934-42F62E71-FAC5-4117-B4A9-3ACC5DB901CE
wd:statement/Q3144934-fd401168-4959-e420-4585-3c4cb94e0ec9
p:P2888 wd:statement/Q3144934-DD990C88-25F3-4350-8C75-DD18905AE13C
wd:statement/Q3144934-DE0372A6-3162-4A27-8154-D5B1BAAC4225
p:P2892 wd:statement/Q3144934-3BDCEB6A-9BD1-4CF1-A26B-E103A1B5AE9E
wd:statement/Q3144934-401D9F57-3555-44FD-B311-8D353BE1782A
p:P31 wd:statement/Q3144934-338C6F5B-D3CE-4E5A-BC3E-6ACB534C87E6
wd:statement/Q3144934-5E9C71C7-2DDE-4726-A042-9817932E67C9
p:P3417 wd:statement/Q3144934-71D648FE-07AD-4D95-9737-5AB6E7A893F0
p:P4229 wd:statement/Q3144934-1E54F0AE-0FA7-4F33-BDF7-9361E7D6A3B4
wd:statement/Q3144934-A503D1D3-BE70-4E5C-861B-4D5DA4DC6AFD
wd:statement/Q3144934-C2B8CB36-CF36-4249-9C59-C699D8835014
p:P4233 wd:statement/Q3144934-31ee0e94-411a-0528-5255-9e82f26494d3
p:P4317 wd:statement/Q3144934-77A2A7B3-DC33-4A1A-8372-AD0802B587CA
p:P486 wd:statement/Q3144934-2B1BE031-FCC4-467A-8E76-E11884D20E75
p:P492 wd:statement/Q3144934-0D8608C4-EC2D-4EDE-8CF7-B25F6F3EB6D7
wd:statement/Q3144934-2B520362-DEDE-4384-9EE2-3AE4DEEE2F7D
p:P5008 wd:statement/Q3144934-6DCC19B0-42B9-4926-B4A5-DF6EF28FC2CD
p:P5270 wd:statement/Q3144934-110F4353-09C3-4AE0-8850-F7EE9A934448
p:P557 wd:statement/Q3144934-24B1DE1B-EDE4-4D43-883F-C66EB8FF0740
p:P604 wd:statement/Q3144934-7BB659DE-7B10-427E-8ACA-E38AF67BF109
p:P6366 wd:statement/Q3144934-017E7E20-E4D1-411E-A602-C20A6173ADD1
wd:statement/Q3144934-58723FC0-B609-44A8-838E-2D084F13254D
wd:statement/Q3144934-C9ED2404-6E05-46E4-8E23-47ACEBF067CB
p:P665 wd:statement/Q3144934-FC3B5A10-6EB7-472A-9658-849BD84A55DE
p:P672 wd:statement/Q3144934-174C6D7F-BFE7-4EFF-AAC7-43C26A7DAEB0
wd:statement/Q3144934-72D2D93D-7ABD-43BD-A15C-3BF4C620D738
wd:statement/Q3144934-DC87B798-DC4D-4ACB-911A-70F24FF1BAE8
p:P699 wd:statement/Q3144934-A278C539-E061-46D5-BD97-4426A10A6530
p:P7807 wd:statement/Q3144934-130C080C-8A05-4BE9-9861-20E3B64EBEC3
p:P973 wd:statement/Q3144934-273087F0-9CE7-418F-BE17-48B28B935EB6
wd:statement/Q3144934-5F130F8F-2D76-46DA-A18F-57B40AA10972
wd:statement/Q3144934-8E814DEF-687A-42B9-9381-5BF7ED21C066
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D006432>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0006507>
p:direct-normalized/P6366 <https://makg.org/entity/2777895808>
<https://makg.org/entity/2908793464>
<https://makg.org/entity/2910309919>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00211>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C16.320.565.618.337>
<http://id.nlm.nih.gov/mesh/C18.452.565.500.480>
<http://id.nlm.nih.gov/mesh/C18.452.648.618.337>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:2352>
wdt:P10283 "C3018783601"
wdt:P11143 "Hereditary haemochromatosis"
wdt:P11956 "1000642"
wdt:P1299 The Gaulic Disease
wdt:P13204 "qxg47wgw"
wdt:P1417 "topic/type-1-hemochromatosis"
wdt:P1542 liver cirrhosis
wdt:P1550 "139498"
"220489"
wdt:P1748 "C84481"
wdt:P1995 endocrinology
hepatology
wdt:P2176 deferoxamine
deferasirox
deferiprone
wdt:P2293 HFE
wdt:P279 iron overload
wdt:P2888 <http://identifiers.org/doid/DOID:2352>
<http://purl.obolibrary.org/obo/DOID_2352>
wdt:P2892 "C0018995"
"C0392514"
wdt:P31 type of disease
rare disease
wdt:P3417 "Hemochromatosis"
wdt:P4229 "E83.11"
"E83.110"
"E83.119"
wdt:P4233 "hemochromatosis"
wdt:P4317 "10746"
wdt:P486 "D006432"
wdt:P492 "231100"
"235200"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0006507"
wdt:P557 "5490"
wdt:P604 "000327"
wdt:P6366 "2777895808"
"2908793464"
"2910309919"
wdt:P665 "H00211"
wdt:P672 "C16.320.565.618.337"
"C18.452.565.500.480"
"C18.452.648.618.337"
wdt:P699 "DOID:2352"
wdt:P7807 "173494020"
wdt:P973 <https://britishlivertrust.org.uk/information-and-support/liver-conditions/haemochromatosis/treatment/>
<https://view-health-screening-recommendations.service.gov.uk/haemochromatosis/>
<https://www.nhs.uk/conditions/haemochromatosis/>
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data from SPARQL profile: Wikidata