Jacobsenov sindrom (Q1677755)

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multiple congenital anomaly caused by deletion on chromosome 11 engleski
uredi
Jezik Oznaka Opis Poznato i kao
bosanski
Jacobsenov sindrom
Opis nije definiran
    engleski
    Jacobsen syndrome
    multiple congenital anomaly caused by deletion on chromosome 11
    • Partial 11Q Monosomy Syndrome
    • JBS
    • JACOBSEN SYNDROME
    • Distal monosomy 11q
    • Chromosome 11Q Deletion Syndrome
    • Distal deletion 11q
    • Monosomy 11qter
    • JACOBSEN SYNDROME; JBS
    • Del(11)(qter)
    • Telomeric deletion 11q
    • 11q Terminal Deletion Disorder
    • Del(11)(q23.3)
    • Jacobsen Syndrome
    • Jacobsen Distal 11q Deletion Syndrome

    Iskazi

    slika
    Jacobsen syndrome patient.JPG
    921 × 1.192; 553 KB
    0 referenci
    otkrivač ili izumitelj
    Petra Jacobsen engleski
    0 referenci
    health specialty engleski
    medicinska genetika
    0 referenci
    kategorija na Commonsu
    Jacobsen syndrome
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    Identifikatori

    MeSH kod
    C15.378.140.855.440
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    C16.131.260.440
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    C16.320.180.440
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    C15.378.243.937.440
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    Disease Ontology ID engleski
    DOID:0111723
    1 referenca
    navedeno u
    Disease Ontology engleski
    pristupljeno
    30 novembar 2020
    Disease Ontology ID engleski
    DOID:0111723
    GARD rare disease ID engleski
    307
    0 referenci
    ICD-11 ID (Foundation) engleski
    27788176
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    Mondo ID engleski
    MONDO_0007838
    0 referenci
    WikiProjectMed ID engleski
    Jacobsen syndrome
    0 referenci
     
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                  Preuzeto iz "https://www.wikidata.org/w/index.php?title=Q1677755&oldid=2180145431"