Owren's disease

Summary

Owren's disease is a rare disease^[1].

Key Facts

• Owren's disease's instance of is recorded as rare disease^[2].
• Owren's disease's instance of is recorded as class of disease^[3].
• Owren's disease's subclass of is recorded as inherited blood coagulation disease^[4].
• Owren's disease's subclass of is recorded as rare hemorrhagic disorder due to a constitutional coagulation factors defect^[5].
• Owren's disease's subclass of is recorded as autosomal recessive disease^[6].
• Owren's disease's subclass of is recorded as blood coagulation disease^[7].
• Owren's disease's MeSH descriptor ID is recorded as D005166^[8].
• Owren's disease's OMIM ID is recorded as 227400^[9].
• Owren's disease's KEGG ID is recorded as H00220^[10].
• Owren's disease's MeSH tree code is recorded as C15.378.100.100.300^[11].
• Owren's disease's MeSH tree code is recorded as C15.378.100.141.300^[12].
• Owren's disease's MeSH tree code is recorded as C15.378.463.300^[13].
• Owren's disease's MeSH tree code is recorded as C16.320.099.300^[14].
• Owren's disease's Disease Ontology ID is recorded as DOID:2216^[15].
• Owren's disease's Orphanet ID is recorded as 326^[16].
• Owren's disease's NCI Thesaurus ID is recorded as C98938^[17].
• Owren's disease's health specialty is recorded as hematology^[18].
• Owren's disease's health specialty is recorded as medical genetics^[19].
• Owren's disease's genetic association is recorded as F5^[20].
• Owren's disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2216^[21].
• Owren's disease's exact match is recorded as http://identifiers.org/doid/DOID:2216^[22].
• Owren's disease's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003225^[23].
• Owren's disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_326^[24].
• Owren's disease's UMLS CUI is recorded as C0015499^[25].
• Owren's disease's Human Phenotype Ontology ID is recorded as HP:0003225^[26].