SHMARQL

acute intermittent porphyria

<http://www.wikidata.org/entity/Q424247>

human disease
rdfs:label
"acute intermittent porphyria"@en
skos:altLabel
"AIP"@en
"AIP - acute intermittent porphyria"@en
"porphyria intermittent acute"@en
"pyrroloporphyria"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:35:37+00:00"^^xsd:dateTime
schema:version 2560167150
wikibase:identifiers 25
27
wikibase:sitelinks 13
wikibase:statements 44
p:P10283 wd:statement/Q424247-31E5B908-2D44-4F86-8D46-7A27A0CDA709
p:P11143 wd:statement/Q424247-05F30F19-A6BD-43DC-BFE3-7DD2D93DB46F
p:P11430 wd:statement/Q424247-5124ccef-47ab-1fba-786b-31375021c8d5
p:P1193 wd:statement/Q424247-451ED257-1F0F-48D2-AD11-F129B1A9C3BB
p:P1199 wd:statement/Q424247-694598d1-43c6-968d-5f61-285ab7a79084
p:P1417 wd:statement/Q424247-1C541802-6FB0-4142-ABE0-7C4681B59919
p:P14914 wd:statement/Q424247-6B83605C-294E-4BEF-80EB-16D18D86C51B
p:P1550 wd:statement/Q424247-F57803EA-7E0B-414E-BA86-89D183F003A7
p:P1748 wd:statement/Q424247-BDB59A00-7799-4D82-8A15-52F940F62646
p:P1995 wd:statement/Q424247-03AD7C1A-BB34-418D-9D5A-9C8E59687EE9
wd:statement/Q424247-3b869b55-424e-7af0-2366-d895e4acb9c2
p:P2176 wd:statement/Q424247-0c800d62-46e1-358c-47e4-87dce6be64ea
wd:statement/Q424247-7824cbdd-46ef-47c5-743c-deddfe6f81e8
wd:statement/Q424247-9cc00e38-4c4c-a7d5-c6ad-eaf1e802f2e0
p:P2293 wd:statement/Q424247-666ceb94-478c-da75-1d84-6782b7e6f1e8
p:P279 wd:statement/Q424247-D7A6F292-7C55-43F8-8222-2ED2BF8198DD
wd:statement/Q424247-e6f2137e-45f8-5e57-e03d-fea89e50dca3
p:P2841 wd:statement/Q424247-B5450502-CA19-4D28-8DCD-51C71F33711E
wd:statement/Q424247-FE01A587-AF6C-43B3-9E3F-75E43EC7D19B
p:P2888 wd:statement/Q424247-9EAC814D-0617-4AD3-9A73-02444E990CD0
wd:statement/Q424247-C510ABFB-A394-49CE-80A2-AF8CEDFC0257
p:P2892 wd:statement/Q424247-B5A9E6A8-94D1-4813-9B73-68CCB4B35C95
p:P31 wd:statement/Q424247-7D6740F0-52B3-4C15-B7FB-E6A06F4FAC75
wd:statement/Q424247-98A65261-5B9E-4C8A-A494-64A93DA6FC61
p:P3827 wd:statement/Q424247-F6B8AB20-2F51-4636-A718-FA08160C012F
p:P4233 wd:statement/Q424247-1a8a526f-4ea6-fa68-fdde-d50930983d25
p:P4317 wd:statement/Q424247-2B710F1D-910C-45EA-82FF-F7B2339E8762
p:P486 wd:statement/Q424247-1B25D1C2-7442-4DF0-A023-21FEBB288B1C
p:P492 wd:statement/q424247-9F1F897D-6D63-48FF-86E7-F054212C1D94
p:P493 wd:statement/q424247-2FC1FB1B-FB97-4ED7-8694-BB6D7552FC65
p:P494 wd:statement/q424247-92523E2B-2DC2-42DA-A93C-A956A980C426
p:P5008 wd:statement/Q424247-C1098C6E-000A-459B-8D4A-C6CF166B7DD2
p:P5270 wd:statement/Q424247-FDDDFC02-330E-4BE6-8062-5A95B9950E0F
p:P557 wd:statement/q424247-B0BDD8A3-557D-4799-BF2F-D461F9857E38
p:P6366 wd:statement/Q424247-2E8C6013-F05E-4B67-944E-C5A73CEFD010
p:P646 wd:statement/Q424247-B4AFD7F2-5AD0-4415-9BAA-A812D7B2B01D
p:P668 wd:statement/q424247-2A62B79A-91F5-4DB9-97C2-FAC4D5C6A989
p:P672 wd:statement/Q424247-15A41859-3948-4F81-B773-1CA1A1EFE577
wd:statement/Q424247-2D7639B9-107E-4DB8-ABBE-680B65C0578B
wd:statement/Q424247-87A85024-2B04-4633-BC09-30119B37CEB6
wd:statement/Q424247-E190FA2F-E138-472C-9394-03D464072668
p:P673 wd:statement/q424247-0536F9DB-369B-4AD6-A4EA-4ED624DCD841
p:P699 wd:statement/Q424247-DFB096CE-D5F5-44D6-A51F-AD38BB4A4EE3
p:P7807 wd:statement/Q424247-06381a56-41bb-8e60-09bd-46a8a56d313a
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D017118>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0008294>
p:direct-normalized/P6366 <https://makg.org/entity/2779028619>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C06.552.830.150>
<http://id.nlm.nih.gov/mesh/C16.320.850.742.150>
<http://id.nlm.nih.gov/mesh/C17.800.827.742.150>
<http://id.nlm.nih.gov/mesh/C18.452.811.400.150>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:3890>
wdt:P10283 "C2779028619"
wdt:P11143 "Acute intermittent porphyria"
wdt:P11430 "DI-00037"
wdt:P1193 0.000005^^xsd:decimal
wdt:P1199 autosomal dominant
wdt:P1417 "science/acute-intermittent-porphyria"
wdt:P14914 "D79276"
wdt:P1550 "79276"
wdt:P1748 "C84536"
wdt:P1995 hematology
neurology
wdt:P2176 Heme arginate
glucose
givosiran
wdt:P2293 HMBS
wdt:P279 porphyria due to ALAD deficiency
wdt:P2841 juvenile onset
adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:3890>
<http://purl.obolibrary.org/obo/DOID_3890>
wdt:P2892 "C0162565"
wdt:P31 type of disease
rare disease
wdt:P3827 "acute-intermittent-porphyria"
wdt:P4233 "acute-intermittent-porphyria"
wdt:P4317 "5732"
wdt:P486 "D017118"
wdt:P492 "176000"
wdt:P493 "277.1"
wdt:P494 "E80.2"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0008294"
wdt:P557 "171"
wdt:P6366 "2779028619"
wdt:P646 "/m/082sss"
wdt:P668 "NBK1193"
wdt:P672 "C06.552.830.150"
"C16.320.850.742.150"
"C17.800.827.742.150"
"C18.452.811.400.150"
wdt:P673 "205220"
wdt:P699 "DOID:3890"
wdt:P7807 "1565229118"
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data from SPARQL profile: Wikidata