Wikidata entity: Q3335671

P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url None ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2293 genetic association ... Q18029674 (TRIM37) TRIM37
P1995 health specialty ... Q327657 (rheumatology) rheumatology
P1995 health specialty ... Q1071953 (medical genetics) medical genetics
P1692 ICD-9-CM String 759.89 ???
P31 instance of ... Q929833 (rare disease) rare disease
P31 instance of ... Q55788864 (developmental defect during embryogenesis) developmental defect during embryogenesis
P31 instance of ... Q112193867 (class of disease) class of disease
P1748 NCI Thesaurus ID String C84906 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q179630 (syndrome) syndrome
P279 subclass of ... Q55785846 (rare genetic developmental defect during embryogenesis) rare genetic developmental defect during embryogenesis
P279 subclass of ... Q10267817 (autosomal recessive disease) autosomal recessive disease
P279 subclass of ... Q55785400 (malformation syndrome with short stature) malformation syndrome with short stature
External Ids
P699Disease Ontology IDDOID:0050436
P557DiseasesDB32892
P646Freebase ID/m/05jtrr
P4317GARD rare disease ID95
P4229ICD-10-CMQ87.1
P665KEGG IDH01289
P486MeSH descriptor IDD050336
P672MeSH tree codeC05.116.099.343.796
P672MeSH tree codeC16.320.240.875
P6366Microsoft Academic ID (discontinued)2779505184
P6366Microsoft Academic ID (discontinued)2910834923
P5270Mondo IDMONDO_0009664
P492OMIM ID253250
P492OMIM ID253250
P1550Orphanet ID2576
P2892UMLS CUIC0524582
P2892UMLS CUIC2931895
P11430UniProt disease IDDI-02001
P11143WikiProjectMed IDMulibrey nanism
P2347YSO ID21960

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