congenital afibrinogenemia
Human disease
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congenital afibrinogenemia
Summary
congenital afibrinogenemia is a class of disease[1]. It draws 6 Wikipedia views per month (class_of_disease category, ranking #626 of 1,968).[2]
Key Facts
- congenital afibrinogenemia's instance of is recorded as class of disease[3].
- congenital afibrinogenemia's subclass of is recorded as Factor I Deficiency[4].
- congenital afibrinogenemia's subclass of is recorded as inherited blood coagulation disease[5].
- congenital afibrinogenemia's subclass of is recorded as autosomal recessive disease[6].
- congenital afibrinogenemia's subclass of is recorded as blood coagulation disease[7].
- congenital afibrinogenemia's MeSH descriptor ID is recorded as D000347[8].
- congenital afibrinogenemia's OMIM ID is recorded as 202400[9].
- congenital afibrinogenemia's ICD-9 ID is recorded as 286.3[10].
- congenital afibrinogenemia's DiseasesDB is recorded as 307[11].
- congenital afibrinogenemia's MedlinePlus ID is recorded as 001313[12].
- congenital afibrinogenemia's KEGG ID is recorded as H00222[13].
- congenital afibrinogenemia's MeSH tree code is recorded as C15.378.100.100.056[14].
- congenital afibrinogenemia's MeSH tree code is recorded as C15.378.100.141.072[15].
- congenital afibrinogenemia's MeSH tree code is recorded as C15.378.463.067[16].
- congenital afibrinogenemia's MeSH tree code is recorded as C16.320.099.056[17].
- congenital afibrinogenemia's Encyclopædia Britannica Online ID is recorded as science/afibrinogenemia[18].
- congenital afibrinogenemia's Orphanet ID is recorded as 98880[19].
- congenital afibrinogenemia's NCI Thesaurus ID is recorded as C98130[20].
- congenital afibrinogenemia's health specialty is recorded as hematology[21].
- congenital afibrinogenemia's genetic association is recorded as FGG[22].
- congenital afibrinogenemia's genetic association is recorded as FGB[23].
- congenital afibrinogenemia's BabelNet ID is recorded as 00021809n[24].
- congenital afibrinogenemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2236[25].
- congenital afibrinogenemia's exact match is recorded as http://identifiers.org/doid/DOID:2236[26].
- congenital afibrinogenemia's UMLS CUI is recorded as C0001733[27].
Why It Matters
congenital afibrinogenemia draws 6 Wikipedia views per month (class_of_disease category, ranking #626 of 1,968).[2]