Wikidata entity: Q275385

P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2293 genetic association ... Q14885224 (PPOX) PPOX
P2293 genetic association ... Q14890978 (HFE) HFE
P1995 health specialty ... Q162606 (endocrinology) endocrinology
P31 instance of ... Q929833 (rare disease) rare disease
P31 instance of ... Q112193867 (class of disease) class of disease
P1199 mode of inheritance ... Q116406 (autosomal dominant) autosomal dominant
P1748 NCI Thesaurus ID String C85219 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q271759 (porphyria) porphyria
P279 subclass of ... Q419897 (porphyria due to ALAD deficiency) porphyria due to ALAD deficiency
P279 subclass of ... Q55788880 (acute hepatic porphyria) acute hepatic porphyria
External Ids
P699Disease Ontology IDDOID:4346
P557DiseasesDB13738
P673eMedicine ID1103846
P1417Encyclopædia Britannica Online IDscience/variegate-porphyria
P646Freebase ID/m/02ktm6
P4317GARD rare disease ID7848
P494ICD-10 IDE80.2
P4229ICD-10-CME80.2
P7807ICD-11 ID (Foundation)1227474618
P7329ICD-11 ID (MMS)5C58.13
P493ICD-9 ID277.1
P3827JSTOR topic ID (archived)variegate-porphyria
P486MeSH descriptor IDD046350
P672MeSH tree codeC06.552.830.625
P672MeSH tree codeC16.320.850.742.625
P672MeSH tree codeC17.800.827.742.625
P672MeSH tree codeC18.452.811.400.625
P6366Microsoft Academic ID (discontinued)2778969481
P5270Mondo IDMONDO_0008297
P492OMIM ID176200
P492OMIM ID176200
P1550Orphanet ID79473
P4233PatientsLikeMe condition IDvariegate-porphyria
P2892UMLS CUIC0162532
P2892UMLS CUIC2936913
P2892UMLS CUIC3149848
P11430UniProt disease IDDI-00928
P11143WikiProjectMed IDVariegate porphyria

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