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cerebrovascular disease English (Q3010352)

Item Discussion
artery disease that is characterized by dysfunction of the blood vessels supplying the brain English
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Language Label Description Also known as
British English
No label defined
No description defined

    Statements

    NDL authority ID
    00568663
    0 references
    subclass of
    central nervous system disease English
    0 references
    vascular disease English
    4 references
    stated in
    Q39116577 (Deleted Item)
    stated in
    Q37380546 (Deleted Item)
    stated in
    Q37271632 (Deleted Item)
    stated in
    Disease Ontology English
    retrieved
    29 November 2020
    Disease Ontology ID
    DOID:6713
    Q576349 (Deleted Item)
    2 references
    stated in
    Q35231770 (Deleted Item)
    stated in
    Disease Ontology English
    retrieved
    29 November 2020
    Disease Ontology ID
    DOID:6713
    Q55788489 (Deleted Item)
    0 references
    Q112193769 (Deleted Item)
    0 references
    Freebase ID
    /m/01l2lr
    1 reference
    stated in
    Q15241312 (Deleted Item)
    publication date
    28 October 2013
    health speciality
    cardiology
    0 references
    Q83042 (Deleted Item)
    0 references
    BNCF Thesaurus
    4954
    1 reference
    stated in
    Q16583225 (Deleted Item)
    Disease Ontology ID
    DOID:6713
    1 reference
    stated in
    Disease Ontology English
    retrieved
    29 November 2020
    Disease Ontology ID
    DOID:6713
    genetic association English
    Q18048631 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=92369
    http://www.genome.gov/gwastudies/index.cfm?gene=SPSB4
    stated in
    Q22330995 (Deleted Item)
    Q29417025 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q18027905 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=3613
    http://www.genome.gov/gwastudies/index.cfm?gene=IMPA2
    stated in
    Q22330995 (Deleted Item)
    Q28943330 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q17816379 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=202
    http://www.genome.gov/gwastudies/index.cfm?gene=AIM1
    stated in
    Q22330995 (Deleted Item)
    Q28943330 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q18034627 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=9734
    http://www.genome.gov/gwastudies/index.cfm?gene=HDAC9
    stated in
    Q22330995 (Deleted Item)
    Q29417129 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q17832572 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=463
    http://www.genome.gov/gwastudies/index.cfm?gene=ZFHX3
    stated in
    Q22330995 (Deleted Item)
    Q29417025 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q14881709 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=9509
    http://www.genome.gov/gwastudies/index.cfm?gene=ADAMTS2
    stated in
    Q22330995 (Deleted Item)
    Q28943400 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q14911781 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=217
    http://www.genome.gov/gwastudies/index.cfm?gene=ALDH2
    stated in
    Q22330995 (Deleted Item)
    Q29417025 (Deleted Item)
    retrieved
    25 Mayıs 2020
    Q18047096 (Deleted Item)
    determination method
    Q1098876 (Deleted Item)
    Q23190853 (Deleted Item)
    1 reference
    reference URL
    https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6713&ncbiId=81792
    http://www.genome.gov/gwastudies/index.cfm?gene=ADAMTS12
    stated in
    Q22330995 (Deleted Item)
    Q28943400 (Deleted Item)
    retrieved
    25 Mayıs 2020
    UMLS CUI English
    C0038454
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    C0007820
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    NCI Thesaurus ID English
    C3390
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    C2938
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    ICD-10-CM English
    I67.9
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    I60-I69
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    I63.9
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    MeSH
    D002561
    named as
    Cerebrovascular Disorders
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    ICD-9-CM
    437.9
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    430-438.99
    1 reference
    stated in
    Disease Ontology English
    retrieved
    15 Mayıs 2019
    Disease Ontology ID
    DOID:6713
    MeSH Code
    C10.228.140.300
    0 references
    C14.907.253
    0 references
    risk factor English
    Q662860 (Deleted Item)
    cause of
    Q217690 (Deleted Item)
    1 reference
    PubMed ID
    27488512
    cause of
    Q223867 (Deleted Item)
    0 references
    KBpedia ID English
    CerebrovascularDisease
    1 reference
    stated in
    Q64139102 (Deleted Item)
    retrieved
    9 July 2020
    ICD-11 (foundation) English
    843843448
    0 references
    BnF ID
    119373558
    named as
    Maladies cérébrovasculaires
    1 reference
    stated in
    Q16583225 (Deleted Item)
    reference URL
    https://thes.bncf.firenze.sbn.it/termine.php?id=4954
    retrieved
    13 Haziran 2021
    Library of Congress authority ID
    sh85022123
    named as
    Cerebrovascular disease
    1 reference
    stated in
    Q16583225 (Deleted Item)
    reference URL
    https://thes.bncf.firenze.sbn.it/termine.php?id=4954
    retrieved
    13 Haziran 2021
    NALT ID
    24058
    0 references
    24052
    0 references
    YSO ID
    1710
    1 reference
    stated in
    Q89345680 (Deleted Item)
    retrieved
    24 November 2021
    National Library of Israel J9U ID
    987007284805305171
    1 reference
    stated in
    Q188915 (Deleted Item)
    instance of
    Q112193867 (Deleted Item)
    0 references
    NKCR AUT ID
    ph138725
    named as
    cerebrovaskulární nemoci
    0 references
     
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