congenital prekallikrein deficiency

Summary

congenital prekallikrein deficiency is a rare disease^[1].

Key Facts

• congenital prekallikrein deficiency's instance of is recorded as rare disease^[2].
• congenital prekallikrein deficiency's instance of is recorded as class of disease^[3].
• congenital prekallikrein deficiency's subclass of is recorded as rare hemorrhagic disorder due to a constitutional coagulation factors defect^[4].
• congenital prekallikrein deficiency's MeSH descriptor ID is recorded as C562725^[5].
• congenital prekallikrein deficiency's OMIM ID is recorded as 612423^[6].
• congenital prekallikrein deficiency's KEGG ID is recorded as H01078^[7].
• congenital prekallikrein deficiency's Orphanet ID is recorded as 749^[8].
• congenital prekallikrein deficiency's ICD-9-CM is recorded as 286.9^[9].
• congenital prekallikrein deficiency's NCI Thesaurus ID is recorded as C99022^[10].
• congenital prekallikrein deficiency's genetic association is recorded as KLKB1^[11].
• congenital prekallikrein deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_749^[12].
• congenital prekallikrein deficiency's UMLS CUI is recorded as C0272339^[13].
• congenital prekallikrein deficiency's ICD-10-CM is recorded as D68.8^[14].
• congenital prekallikrein deficiency's GARD rare disease ID is recorded as 4477^[15].
• congenital prekallikrein deficiency's Mondo ID is recorded as MONDO_0012901^[16].
• congenital prekallikrein deficiency's Genetics Home Reference Conditions ID is recorded as prekallikrein-deficiency^[17].
• congenital prekallikrein deficiency's ICD-11 ID is recorded as 2010669339^[18].
• congenital prekallikrein deficiency's UniProt disease ID is recorded as DI-02188^[19].