SHMARQL

tyrosinemia type III

<http://www.wikidata.org/entity/Q7861692>

tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine
rdfs:label
"tyrosinemia type III"@en
skos:altLabel
"Hereditary tyrosinemia, Type III"@en
"High tyrosinemia"@en
"Hypertyrosinemia type III"@en
"TYRSN3"@en
schema:description
"tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine"@en
schema:dateModified "2026-10-24T00:31:28+00:00"^^xsd:dateTime
schema:version 2560166540
wikibase:identifiers 12
wikibase:sitelinks 3
wikibase:statements 28
p:P11430 wd:statement/Q7861692-379595f5-4bc8-43b1-7f10-2ae33881a2d1
p:P1193 wd:statement/Q7861692-E12852AF-74C2-46C9-AAE9-8EF4EFA74CC1
p:P1325 wd:statement/Q7861692-210298BE-45D3-4702-A64A-12161E0406F8
p:P14914 wd:statement/Q7861692-70AB0C34-FB86-4E64-A3D4-4B6623F5F1C0
p:P1550 wd:statement/Q7861692-c9be0ab0-40f9-a3f6-dd4f-2f38aac4cacf
p:P1995 wd:statement/Q7861692-CADEE5E4-CB1B-41C1-A801-B6D3C5AC7415
p:P2176 wd:statement/Q7861692-5E6E69A1-65AC-4976-964A-031DF7D6A565
wd:statement/Q7861692-70F068AB-F2AB-4F9D-ADA0-5C10BD8DA8CE
p:P2293 wd:statement/Q7861692-479880B6-B5CE-492B-B896-F8785A6B6019
p:P279 wd:statement/Q7861692-bad9c065-47cc-e304-c60d-e60acac81139
p:P2841 wd:statement/Q7861692-66FB11B8-9450-4CCE-8370-36DC7F371595
wd:statement/Q7861692-89883947-A7B7-409A-B687-C1DEB64EFA30
p:P2888 wd:statement/Q7861692-8958BEBE-AB77-4D6E-9005-FB6318740551
wd:statement/Q7861692-F7C65BA9-87BD-4255-B127-91CA281195C0
p:P31 wd:statement/Q7861692-00686467-79D7-4AE6-A182-B5A2938E4F6C
wd:statement/Q7861692-A9465BAE-B92D-4B61-AE67-CB2CD1BC3DB0
wd:statement/Q7861692-F7853DEC-02A2-430F-84C7-E51822A51E6D
p:P4233 wd:statement/Q7861692-6f18709d-49ce-688d-f0c4-c80371555be1
p:P4317 wd:statement/Q7861692-FD755AD2-0320-4A6A-8278-7CD4D0E38BDC
p:P492 wd:statement/q7861692-E3CFA9C6-1025-4928-9275-8E0A56885B5F
p:P493 wd:statement/q7861692-FDE3AE36-AAFD-49BE-A296-A701363D180A
p:P494 wd:statement/q7861692-3DAE1E76-0541-4E89-860C-9FC3E498B59B
p:P5008 wd:statement/Q7861692-FF2EC54D-C582-4B3A-8D68-7505948528FD
p:P5270 wd:statement/Q7861692-FB1897DA-5938-440E-9886-529BE50983B0
p:P557 wd:statement/Q7861692-33976630-02AD-4FA0-BF3F-FC4D82C58F5A
p:P6366 wd:statement/Q7861692-9530FC5D-6D00-4294-BE47-BC6DF6639967
p:P6532 wd:statement/Q7861692-33403C5E-EC97-41A1-9E31-D4E47F137AC7
p:P699 wd:statement/Q7861692-A9D98C93-0047-41D0-A0AA-0413FA03606C
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010162>
p:direct-normalized/P6366 <https://makg.org/entity/2775904740>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050727>
wdt:P11430 "DI-01109"
wdt:P1193 0.000001^^xsd:decimal
wdt:P1325 <http://www.nanbyou.or.jp/entry/4696>
wdt:P14914 "D69723"
wdt:P1550 "69723"
wdt:P1995 endocrinology
wdt:P2176 nitisinone
sodium ascorbate
wdt:P2293 HPD
wdt:P279 tyrosinemia
wdt:P2841 neonatal onset
infantile onset
wdt:P2888 <http://identifiers.org/doid/DOID:0050727>
<http://purl.obolibrary.org/obo/DOID_0050727>
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P4233 "tyrosinemia-type-iii"
wdt:P4317 "10332"
wdt:P492 "276710"
wdt:P493 "270.2"
wdt:P494 "E70.2"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010162"
wdt:P557 "29836"
wdt:P6366 "2775904740"
wdt:P6532 wd:Q39209282
wdt:P699 "DOID:0050727"
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