multiple system atrophy

neurodegenerative disorder characterized by autonomic failure, parkinsonism, cerebellar impairment and corticospinal signs, with a median survival of 6-9 years

Wikidata entity: Q1541975

Wikimedia Commons category is Multiple system atrophy

P373 Commons category String Multiple system atrophy ???
P2176 drug or therapy used for treatment ... Q907853 (droxidopa) droxidopa
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 Ontology Lookup Service (OLS) ???
P1325 external data available at URL Url None ???
P2293 genetic association ... Q18038726 (COQ2) COQ2
P1995 health specialty ... Q83042 (neurology) neurology
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q42303753 (designated intractable/rare disease) designated intractable/rare disease
P1748 NCI Thesaurus ID String C84909 ???
P1748 NCI Thesaurus ID String C85066 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P460 said to be the same as ... Q2280546 (Shy-Drager syndrome) Shy-Drager syndrome
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q1755122 (neurodegeneration) neurodegeneration
P279 subclass of ... Q2376264 (synucleinopathy) synucleinopathy
External Ids
P1617BBC Things IDea96c475-306b-45d3-a281-74b433b665c2
P8072CAB ID218406
P699Disease Ontology IDDOID:4752
P557DiseasesDB8441
P673eMedicine ID1154583
P10565Encyclopedia of China (Third Edition) ID133685
P11956Experimental Factor Ontology ID1001050
P646Freebase ID/m/03j8_2
P4317GARD rare disease ID7079
P7464Genetics Home Reference Conditions IDmultiple-system-atrophy
P494ICD-10 IDG232
P4229ICD-10-CMG90.3
P7807ICD-11 ID (Foundation)1890931931
P7329ICD-11 ID (MMS)8D87.0
P493ICD-9 ID333.0
P3827JSTOR topic ID (archived)multiple-system-atrophy
P665KEGG IDH01614
P604MedlinePlus ID000757
P604MedlinePlus ID000757
P486MeSH descriptor IDD019578
P672MeSH tree codeC10.177.575.550
P672MeSH tree codeC10.228.140.079.612
P672MeSH tree codeC10.228.662.550
P672MeSH tree codeC10.574.928.625
P5270Mondo IDMONDO_0007803
P7995NHS Health A to Z IDmultiple-system-atrophy
P492OMIM ID146500
P492OMIM ID146500
P1550Orphanet ID102
P1461Patientplus IDmultiple-system-atrophy
P4233PatientsLikeMe condition IDmsa
P2892UMLS CUIC0020651
P2892UMLS CUIC0037019
P2892UMLS CUIC0393571
P2892UMLS CUIC0393911
P2892UMLS CUIC3714927
P11430UniProt disease IDDI-03867
P11143WikiProjectMed IDMultiple system atrophy
P2347YSO ID22097

Why not click here or view trends?

log id: 5754485