Wolff–Parkinson–White syndrome

congenital syndrome characterized by additional electrical pathways causing electrical conduction problems in the heart, leading to sporadic episodes of tachycardia and other symptoms.

Wikidata entity: Q925092



Wikimedia Commons category is Wolff–Parkinson–White syndrome

P689 afflicts ... Q72711 (electrical conduction system of the heart) electrical conduction system of the heart
P373 Commons category String Wolff–Parkinson–White syndrome ???
P2176 drug or therapy used for treatment ... Q190012 (adenosine) adenosine
P2176 drug or therapy used for treatment ... Q216935 (lidocaine) lidocaine
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2888 exact match Url None ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2293 genetic association ... Q18040277 (PRKAG2) PRKAG2
P1995 health specialty ... Q10379 (cardiology) cardiology
P1692 ICD-9-CM String 426.7 ???
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q929833 (rare disease) rare disease
P138 named after ... Q366363 (Paul Dudley White) Paul Dudley White
P138 named after ... Q3182251 (John Parkinson) John Parkinson
P138 named after ... Q3263315 (Louis Wolff) Louis Wolff
P1748 NCI Thesaurus ID String C35132 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P5555 schematic CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/WPW.jpeg ???
P5555 schematic CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/Wpw2%20%28CardioNetworks%20ECGpedia%29.svg ???
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q200779 (genetic disease) genetic disease
P279 subclass of ... Q1361515 (heart conduction disease) heart conduction disease
P279 subclass of ... Q2064167 (pre-excitation syndrome) pre-excitation syndrome
External Ids
P268Bibliothèque nationale de France ID12173227c
P508BNCF Thesaurus ID24315
P699Disease Ontology IDDOID:384
P557DiseasesDB14186
P673eMedicine ID159222
P11956Experimental Factor Ontology ID1001450
P646Freebase ID/m/02220s
P4317GARD rare disease ID7897
P3841Human Phenotype Ontology IDHP:0001716
P4229ICD-10-CMI45.6
P7807ICD-11 ID (Foundation)1091030330
P7329ICD-11 ID (MMS)BC81.4
P665KEGG IDH01154
P244Library of Congress authority IDsh85147229
P604MedlinePlus ID000151
P604MedlinePlus ID000151
P486MeSH descriptor IDD014927
P672MeSH tree codeC14.280.067.780.977
P672MeSH tree codeC14.280.123.750.977
P672MeSH tree codeC16.131.240.400.980
P5270Mondo IDMONDO_0008685
P8189National Library of Israel J9U ID987007558557405171
P349NDL Authority ID00576080
P7995NHS Health A to Z IDwolff-parkinson-white-syndrome
P492OMIM ID194200
P492OMIM ID194200
P10283OpenAlex IDC2909624804
P1550Orphanet ID907
P1461Patientplus IDWolff-Parkinson-White-Syndrome
P4233PatientsLikeMe condition IDwolff-parkinson-white
P2892UMLS CUIC0032915
P2892UMLS CUIC0043202
P2892UMLS CUIC0264897
P2892UMLS CUIC0392470
P11430UniProt disease IDDI-01150
P11143WikiProjectMed IDWolff–Parkinson–White syndrome
P13591Yale LUX IDconcept/ed6e655c-dcbf-48f1-9dce-9a2e6632a0f1

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