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Your query: Author Sysno/Doc.kind = "^sllk_un_auth d053549 250m^"
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  1. 1.keratín-6

    Subject h.keratín-6
    Subject h.Keratin-6
    Scope note in EnglishA type II keratin found associated with KERATIN-16 or KERATIN-17 in rapidly proliferating squamous epithelial tissue. Mutations in gene for keratin-6A and keratin-6B have been associated with PACHYONYCHIA CONGENITA, TYPE 1 and PACHYONYCHIA CONGENITA, TYPE 2 respectively.
    See also reference (FX) in Slovak pachyonychia congenita
    See also reference (FX) in English Pachyonychia Congenita
    Links (1) - MeSH descriptor
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  2. 2.keratín-17

    Subject h.keratín-17
    Subject h.Keratin-17
    Scope note in EnglishA type I keratin found associated with KERATIN-6 in rapidly proliferating squamous epithelial tissue. Mutations in the gene for keratin-17 have been associated with PACHYONYCHIA CONGENITA, TYPE 2.
    See also reference (FX) in Slovak pachyonychia congenita
    steatocystoma multiplex
    See also reference (FX) in English Pachyonychia Congenita
    Steatocystoma Multiplex
    Links (2) - MeSH descriptor
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  3. 3.nechty deformované

    Subject h.nechty deformované
    Subject h.Nails, Malformed
    Entry termsnechty malformované
    malformácie nechtov
    abnormality nechtové
    nechty abnormálne
    onychauxis
    onychauxia
    onychogryphosis
    onychogrypóza
    pachyonýchia
    English X referencesOnychauxis
    Onychogryposis
    Scope note in EnglishDeformities in nail structure or appearance, including hypertrophy, splitting, clubbing, furrowing, etc. Genetic diseases such as PACHYONYCHIA CONGENITA can result in malformed nails.
    Links (2) - ARTICLES
    (1) - MeSH descriptor
    (1) - ELECTRONIC RESOURCES
    (3) - BOOKS
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