Cloustonova hidrotska ektodermna displazija (Q5135822)

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Human disease engleski
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Jezik Oznaka Opis Poznato i kao
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Cloustonova hidrotska ektodermna displazija
Opis nije definiran
    engleski
    Clouston syndrome
    Human disease
    • Clouston's syndrome
    • Hidrotic ectodermal dysplasia syndrome (disorder)
    • hidrotic ectodermal dysplasia
    • Clouston's hidrotic ectodermal dysplasia
    • Hidrotic ectodermal dysplasia syndrome
    • Ectodermal Dysplasia 2, Clouston Type
    • Clouston Hidrotic Ectodermal Dysplasia
    • CLOUSTON SYNDROME
    • Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
    • Ectodermal Dysplasia, Hidrotic, 2
    • Ectodermal Dysplasia, Hidrotic, 2, Formerly

    Iskazi

    je
    rijetka bolest
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    klasa bolesti
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    je podklasa od
    autosomal dominant disease engleski
    1 referenca
    navedeno u
    Disease Ontology engleski
    pristupljeno
    30 novembar 2020
    Disease Ontology ID engleski
    DOID:14693
    ectodermal dysplasia engleski
    1 referenca
    navedeno u
    Disease Ontology engleski
    pristupljeno
    30 novembar 2020
    Disease Ontology ID engleski
    DOID:14693
    health specialty engleski
    Dermatologija
    0 referenci
    medicinska genetika
    0 referenci
    kategorija na Commonsu
    Clouston's hidrotic ectodermal dysplasia
    0 referenci

    Identifikatori

    KEGG ID engleski
    H00648
    0 referenci
    Disease Ontology ID engleski
    DOID:14693
    1 referenca
    navedeno u
    Disease Ontology engleski
    pristupljeno
    30 novembar 2020
    Disease Ontology ID engleski
    DOID:14693
    GARD rare disease ID engleski
    2056
    1 referenca
    navedeno u
    Disease Ontology engleski
    pristupljeno
    15 maj 2019
    Disease Ontology ID engleski
    DOID:14693
    ICD-11 (foundation) engleski
    1811429982
    0 referenci
    ICD-11 ID (MMS) engleski
    LD27.03
    subjekt imenovan kao
    Hidrotic ectodermal dysplasia, Clouston type
    0 referenci
    Microsoft Academic ID
    2778009260
    0 referenci
    2910808432
    0 referenci
    Mondo ID engleski
    MONDO_0007510
    0 referenci
    UniProt disease ID engleski
    DI-00431
    0 referenci
     
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