About: PAPA syndrome

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin

Attributes	Values
rdf:type	Item
owl:sameAs	PAPA syndrome
description	genetycznie uwarunkowany zespół chorobowy (pl) Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin (en)
exact match	wds:Q7118181-0DBE3396-2F33-4203-8321-22979BA7775B wds:Q7118181-7AB7910F-1F5E-4AD9-84C1-557B2F01455A
exact match	http://purl.obolibrary.org/obo/DOID_0080519 http://www.orpha.net/ORDO/Orphanet_69126
Mondo ID	wds:Q7118181-920A6ACA-A03C-4B25-BBE6-08DE8D8A972E
DiseasesDB	wds:q7118181-E8C30246-62D5-4991-9E5E-F4B00C39EAC0
Disease Ontology ID	wds:Q7118181-B48F181C-7C89-4EBB-8521-87E039F56986
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0011462
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0080519
Mondo ID	MONDO_0011462
DiseasesDB	32724
Disease Ontology ID	DOID:0080519
rdfs:label	PAPA sendromu (tr) PAPA syndrome (en) PAPA-Syndrom (de) PAPA-syndroom (nl) Sindrome PAPA (it) Síndrome PAPA (es) Zespół PAPA (pl) سندرم پاپا (fa) متلازمة بابا (ar) syndrome d'arthrite purulente-pyoderma gangrenosum-acné (fr)
skos:prefLabel	PAPA sendromu (tr) PAPA syndrome (en) PAPA-Syndrom (de) PAPA-syndroom (nl) Sindrome PAPA (it) Síndrome PAPA (es) Zespół PAPA (pl) سندرم پاپا (fa) متلازمة بابا (ar) syndrome d'arthrite purulente-pyoderma gangrenosum-acné (fr)
name	PAPA sendromu (tr) PAPA syndrome (en) PAPA-Syndrom (de) PAPA-syndroom (nl) Sindrome PAPA (it) Síndrome PAPA (es) Zespół PAPA (pl) سندرم پاپا (fa) متلازمة بابا (ar) syndrome d'arthrite purulente-pyoderma gangrenosum-acné (fr)
instance of	wds:Q7118181-3281F0D9-7D2C-4FBC-A886-9EBC3FA7F8F2 wds:Q7118181-800FC3C1-FD93-4787-A54E-EAC018B68864 wds:Q7118181-8BF545EF-6E7B-4DB5-93E0-CECB7937FFA6
instance of	class of disease rare disease designated intractable/rare disease
subclass of	wds:Q7118181-0B221696-BEE3-4D01-9611-92DA71361269 wds:Q7118181-4042C29E-3BC6-4F1B-B38C-0142CCFD755C wds:Q7118181-4680D6AA-D238-4B0C-8E4C-6D8DDD245439 wds:Q7118181-4C5E4D40-A511-4B3E-AEAB-0025DECEFE0E wds:Q7118181-9142c045-4817-a63b-c8b7-928635eab71e wds:Q7118181-C1D86676-948A-4DC6-BBE8-59836CC4BDC1 wds:Q7118181-C2CB15B6-A06D-4BBB-B10F-94D0D64E7A1F wds:Q7118181-D3294C7D-0167-4BA0-86BB-5931C3017C28
subclass of	syndrome reactive neutrophilic dermatose genodermatosis genetic systemic or rheumatologic disease autosomal dominant disease autoinflammatory syndrome with immune deficiency autoinflammatory syndrome with skin involvement pyogenic autoinflammatory syndrome
KEGG ID	wds:Q7118181-37BF16AA-6D7B-4C80-A507-1C57FD7F804F
KEGG ID	http://www.kegg.jp/entry/H00287
KEGG ID	H00287
UniProt disease ID	wds:Q7118181-5d6e52d7-4bc8-2cb6-5998-5baeda871e15
Orphanet ID	wds:Q7118181-0c6e8427-48f7-ee60-cfac-03452198602a wds:Q7118181-F0B56DF2-3747-4834-B3B3-2E588A8474DE
genetic association	wds:Q7118181-57D7D94F-5E42-4934-B7C9-5FE3D096CE01
GARD rare disease ID	wds:Q7118181-6630074B-7C28-4A0D-B10E-B7F4A247BB70
OMIM ID	wds:Q7118181-35C5272F-776B-4739-96DF-A0327D8DF2D4 wds:q7118181-FFE51292-60A0-44B7-9D45-9AEE87D60A0E
UniProt disease ID	DI-02127
Orphanet ID	69126
genetic association	PSTPIP1
GARD rare disease ID	9176
OMIM ID	604416
skos:altLabel	Pyoderma gangrenosum (en) FRA (en) Pyogenic arthritis (en) Acne syndrome (en) Familial Recurrent Arthritis (en) Sindrome PAPA (es) PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE (en) pyogenic arthritis, pyoderma gangrenosum and acne (en)
external data available at URL	wds:Q7118181-69F292B3-DE3E-459E-813F-F37A4BCB1CEC
NCI Thesaurus ID	wds:Q7118181-49953CF9-3DBE-4B9E-B517-717B3D033B3A
UMLS CUI	wds:Q7118181-8FD7A7B5-931A-4339-B3AF-4BA955483527
MeSH descriptor ID	wds:Q7118181-14130bb5-4893-73c1-dcfc-20ff6ffaca9a
on focus list of Wikimedia project	wds:Q7118181-90067F59-29AB-4105-B218-8CDDC954EB11
Microsoft Academic ID	wds:Q7118181-01F8F190-C8DF-4FAD-A28F-4A9CCD2B19FD
ICD-11 (foundation)	wds:Q7118181-15A331BB-B43B-4B3C-9A9B-4531ECEBDB2F
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C536253
Microsoft Academic ID	https://makg.org/entity/2778274274

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