factor XIII deficiency
Human disease
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Summary
factor XIII deficiency is a rare disease[1]. It draws 103 Wikipedia views per month (rare disease category, ranking #233 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: inherited blood coagulation disease[4], rare hemorrhagic disorder due to a constitutional coagulation factors defect[5]
- Prevalence: 0.000001[6]
- ICD-9-CM: 286.3[7]
- NCI Thesaurus ID: C131633[8], C98941[9]
- Health specialty: hematology[10]
- Genetic association: F13A1[11], F13B[12]
- Age of onset: any age[13]
- Exact match: http://purl.obolibrary.org/obo/DOID_2211[14], http://identifiers.org/doid/DOID:2211[15], http://www.orpha.net/ORDO/Orphanet_331[16]
- On focus list of Wikimedia project: WikiProject Medicine[17]
- Has phenotype: ecchymosis[18], cerebral hemorrhage[19], Q141815118[20], hemarthrosis[21], menorrhagia[22], bleeding gums[23], nosebleed[24], postpartum hemorrhage[25], liver failure[26], inflammatory bowel diseases[27], myeloid leukemia[28]
- P14914: D00331[29]
Why It Matters
factor XIII deficiency is known by 10 alternative names across languages and contexts.[30]