acute intermittent porphyria

human disease

Wikidata entity: Q424247

P2176 drug or therapy used for treatment ... Q407972 (chlorpromazine) chlorpromazine
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2293 genetic association ... Q14904818 (HMBS) HMBS
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 C84536 ???
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
External Ids
P699Disease Ontology IDDOID:3890
P557DiseasesDB171
P673eMedicine ID205220
P1417Encyclopædia Britannica Online IDscience/acute-intermittent-porphyria
P646Freebase ID/m/082sss
P4317GARD rare disease ID5732
P668GeneReviews IDNBK1193
P494ICD-10 IDE80.2
P7807ICD-11 ID (Foundation)1565229118
P493ICD-9 ID277.1
P3827JSTOR topic ID (archived)acute-intermittent-porphyria
P486MeSH descriptor IDD017118
P672MeSH tree codeC06.552.830.150
P672MeSH tree codeC16.320.850.742.150
P672MeSH tree codeC17.800.827.742.150
P672MeSH tree codeC18.452.811.400.150
P6366Microsoft Academic ID (discontinued)2779028619
P5270Mondo IDMONDO_0008294
P492OMIM ID176000
P492OMIM ID176000
P10283OpenAlex IDC2779028619
P1550Orphanet ID79276
P4233PatientsLikeMe condition IDacute-intermittent-porphyria
P2892UMLS CUIC0162565
P11430UniProt disease IDDI-00037
P11143WikiProjectMed IDAcute intermittent porphyria

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