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hemophilia B English (Q2562598)

Item Discussion
An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. English
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Language Label Description Also known as
British English
No label defined
No description defined

    Statements

    OMIM
    306900
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    Freebase ID
    /m/01cbkb
    1 reference
    stated in
    Q15241312 (Deleted Item)
    publication date
    28 October 2013
    Patientplus
    haemophilia-b-factor-ix-deficiency
    1 reference
    reference URL
    http://www.patient.co.uk/patientplus/f.htm
    Disease Ontology ID
    DOID:12259
    0 references
    NCI Thesaurus ID English
    C26721
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    subclass of
    Q18971506 (Deleted Item)
    of
    Q425360 (Deleted Item)
    0 references
    Q18555031 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    Q55010090 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 November 2020
    Disease Ontology ID
    DOID:12259
    Q890200 (Deleted Item)
    1 reference
    stated in
    Disease Ontology English
    retrieved
    30 November 2020
    Disease Ontology ID
    DOID:12259
    Q112193769 (Deleted Item)
    0 references
    UMLS CUI English
    C0008533
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    Quora topic ID
    Hemophilia-B
    1 reference
    stated in
    Q51711 (Deleted Item)
    JSTOR topic ID
    hemophilia-b
    0 references
    Commons category
    Hemophilia B
    0 references
    ICD-10-CM English
    D67
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    GARD rare disease ID
    8732
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    mode of inheritance
    X-linked recessive English
    1 reference
    stated in
    Q62606821 (Deleted Item)
    Genetics Home Reference Conditions ID English
    hemophilia
    Encyclopædia Britannica Online ID
    science/hemophilia-B
    0 references
    MeSH
    D002836
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    ICD-9-CM
    286.1
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 May 2019
    Disease Ontology ID
    DOID:12259
    MeSH Code
    C15.378.100.100.510
    0 references
    C15.378.100.141.510
    0 references
    C15.378.463.510
    0 references
    C16.320.099.510
    0 references
    C16.320.322.235
    0 references
    Microsoft Academic ID
    2777081929
    0 references
    2909704213
    0 references
    ID (MMS) English
    3B11.0
    named as
    Haemophilia B
    0 references
    ICD-11 (foundation) English
    1901375668
    0 references
    Orphanet ID
    98879
    0 references
    WordNet 3.1 Synset ID
    14194469-n
    0 references
    OpenAlex ID
    C2777081929
    1 reference
    stated in
    Q107507571 (Deleted Item)
    retrieved
    26 January 2022
    reference URL
    https://docs.openalex.org/download-snapshot/snapshot-data-format
    ScienceDirect topic ID English
    nursing-and-health-professions/hemophilia-b
    0 references
    DeCS ID
    2885
    0 references
    instance of
    Q112193867 (Deleted Item)
    0 references
     
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