Dysfibrinogenemia
Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen
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Dysfibrinogenemia
Summary
Dysfibrinogenemia is a class of disease[1]. Dysfibrinogenemia draws 12 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).[2]
Key Facts
- Dysfibrinogenemia's instance of is recorded as class of disease[3].
- Dysfibrinogenemia's subclass of is recorded as fibrinogen abnormality[4].
- Dysfibrinogenemia's OMIM ID is recorded as 616004[5].
- Dysfibrinogenemia's Orphanet ID is recorded as 98881[6].
- Dysfibrinogenemia's ICD-9-CM is recorded as 286.3[7].
- Dysfibrinogenemia's NCI Thesaurus ID is recorded as C131659[8].
- Dysfibrinogenemia's genetic association is recorded as FGG[9].
- Dysfibrinogenemia's genetic association is recorded as FGA[10].
- Dysfibrinogenemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_248408[11].
- Dysfibrinogenemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_335[12].
- Dysfibrinogenemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98881[13].
- Dysfibrinogenemia's UMLS CUI is recorded as C1260903[14].
- Dysfibrinogenemia's UMLS CUI is recorded as C0272350[15].
- Dysfibrinogenemia's UMLS CUI is recorded as C5681639[16].
- Dysfibrinogenemia's ICD-10-CM is recorded as D68.2[17].
- Dysfibrinogenemia's PatientsLikeMe condition ID is recorded as dysfibrinogenemia[18].
- Dysfibrinogenemia's GARD rare disease ID is recorded as 2004[19].
- Dysfibrinogenemia's Mondo ID is recorded as MONDO_0014452[20].
- Dysfibrinogenemia's Microsoft Academic ID is recorded as 2777902675[21].
- Dysfibrinogenemia's ICD-11 ID is recorded as 815934276[22].
- Dysfibrinogenemia's UniProt disease ID is recorded as DI-04218[23].
Why It Matters
Dysfibrinogenemia draws 12 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).[2]