hemophilia C

GPTKB entity

Statements (23)
Predicate Object
gptkbp:instanceOf genetic disorder
bleeding disorder
gptkbp:alsoKnownAs gptkb:Rosenthal_syndrome
gptkbp:causedBy factor XI deficiency
gptkbp:diagnosedBy prolonged activated partial thromboplastin time
gptkbp:distinctFrom gptkb:hemophilia_B
gptkb:hemophilia_A
gptkbp:firstDescribed gptkb:Walter_Rosenthal
1953
https://www.w3.org/2000/01/rdf-schema#label hemophilia C
gptkbp:inheritance autosomal recessive
gptkbp:involvedIn gptkb:F11_gene
gptkbp:locatedOnChromosome gptkb:chromosome_4
gptkbp:MeSH_ID D006470
gptkbp:OMIM 612416
gptkbp:prevalence higher in Ashkenazi Jews
gptkbp:symptom prolonged bleeding
menorrhagia
postoperative bleeding
gptkbp:treatment antifibrinolytic agents
fresh frozen plasma
gptkbp:bfsParent gptkb:hemophilia_A
gptkbp:bfsLayer 5