Owren's disease
Human disease
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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 is a type of inherited blood coagulation disease[4].
- Owren's disease is a type of rare hemorrhagic disorder due to a constitutional coagulation factors defect[5].
- Owren's disease is a type of autosomal recessive disease[6].
- Owren's disease is a type of blood coagulation disease[7].
- Owren's disease's NCI Thesaurus ID is recorded as C98938[8].
- Owren's disease's health specialty is recorded as hematology[9].
- Owren's disease's health specialty is recorded as medical genetics[10].
- Owren's disease's genetic association is recorded as F5[11].
- Owren's disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2216[12].
- Owren's disease's exact match is recorded as http://identifiers.org/doid/DOID:2216[13].
- Owren's disease's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003225[14].
- Owren's disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_326[15].
- Owren's disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].