Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb: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 |
| 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
|
| https://www.w3.org/2000/01/rdf-schema#label |
hemophilia C
|