Camurati-Engelmann disease

rare disease

Wikidata entity: Q498487

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 ... Q14904613 (TGFB1) TGFB1
P1995 health specialty ... Q1071953 (medical genetics) medical genetics
P1692 ICD-9-CM String 756.59 ???
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 C84610 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q1225194 (monogenic disease) monogenic disease
P279 subclass of ... Q1233526 (osteosclerosis) osteosclerosis
P279 subclass of ... Q55788814 (primary bone dysplasia with increased bone density) primary bone dysplasia with increased bone density
External Ids
P699Disease Ontology IDDOID:4997
P557DiseasesDB4301
P1417Encyclopædia Britannica Online IDscience/progressive-diaphyseal-dysplasia
P646Freebase ID/m/03qkxbv
P4317GARD rare disease ID1072
P668GeneReviews IDNBK1156
P7464Genetics Home Reference Conditions IDcamurati-engelmann-disease
P3841Human Phenotype Ontology IDHP:0003034
P4229ICD-10-CMQ78.3
P493ICD-9 ID756.59
P665KEGG IDH00434
P486MeSH descriptor IDD003966
P672MeSH tree codeC05.116.099.708.180
P672MeSH tree codeC16.320.144
P6366Microsoft Academic ID (discontinued)2777008563
P5270Mondo IDMONDO_0007542
P492OMIM ID131300
P492OMIM ID131300
P492OMIM ID606631
P492OMIM ID606631
P1550Orphanet ID1328
P2892UMLS CUIC0011989
P2892UMLS CUIC2931842
P11430UniProt disease IDDI-01314
P11143WikiProjectMed IDCamurati–Engelmann disease

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