Factor I Deficiency

Summary

Factor I Deficiency is a class of disease^[1]. It draws 6 Wikipedia views per month (class_of_disease category, ranking #630 of 1,968).^[2]

Key Facts

• Factor I Deficiency's instance of is recorded as class of disease^[3].
• Factor I Deficiency's subclass of is recorded as fibrinogen abnormality^[4].
• Factor I Deficiency's subclass of is recorded as inherited blood coagulation disease^[5].
• Factor I Deficiency's subclass of is recorded as immunodeficiency due to a complement regulatory deficiency^[6].
• Factor I Deficiency's symptoms and signs is recorded as Hypofibrinogenemia^[7].
• Factor I Deficiency's Orphanet ID is recorded as 335^[8].
• Factor I Deficiency's genetic association is recorded as FGA^[9].
• Factor I Deficiency's genetic association is recorded as FGB^[10].
• Factor I Deficiency's genetic association is recorded as FGG^[11].
• Factor I Deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_335^[12].
• Factor I Deficiency's UMLS CUI is recorded as C2062367^[13].
• Factor I Deficiency's ICD-10-CM is recorded as D68.2^[14].
• Factor I Deficiency's GARD rare disease ID is recorded as 2320^[15].
• Factor I Deficiency's Mondo ID is recorded as MONDO_0018060^[16].
• Factor I Deficiency's ICD-11 ID is recorded as 3B14.0^[17].
• Factor I Deficiency's ICD-11 ID is recorded as 1452989457^[18].
• Factor I Deficiency's OpenAlex ID is recorded as C2910129229^[19].

Why It Matters

Factor I Deficiency draws 6 Wikipedia views per month (class_of_disease category, ranking #630 of 1,968).^[2]