Disease #01328 (F8D (deficiency, factor VIII, hereditary (F8D)), OMIM:134500)

Official abbreviation F8D
Name deficiency, factor VIII, hereditary (F8D)
OMIM ID 134500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2017-01-27 15:15:23 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00104712 08605341-PatS143 PubMed: Naylor 1996 affected male, mother and other ascendant relatives deceased, family history indicates patient's mother/maternal grandmother were obligatory cariers of hemophilia M - United Kingdom (Great Britain) - >58y - - - F8D see paper; ..., severe hemophilia, low-level intermittent inhibitor, max titer last 8y 3.5 Bethesda units F8 F8 3 1 Johan den Dunnen
00391136 - - - F - (United States) - - - - - F8D dvt GORAB GORAB 1 1 Jessica Easterday
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