Number of the records: 1  

laminopatie

  1. Topical termlaminopatie
    See linkLMNA-Associated Diseases (UF)
    LMNA-Linked Diseases (UF)
    onemocnění asociovaná s genem LMNA (UF)
    See alsogenetické nemoci vrozené
    autozomální Emery-Dreifuss muskulární dystrofie
    dilatační kardiomyopatie
    familiární parciální lipodystrofie
    progerie
    Linking entryLaminopathies
    ConspectC16. - 320. - 488
    NoteCongenital neuromuscular and muscular dystrophy diseases associated with mutations in the LAMIN TYPE A (Lamin A/C or LMNA gene). It includes CARDIOMYOPATHY, DILATED, 1A; CHARCOT-MARIE-TOOTH DISEASE, type 2B1; EMERY-DREIFUSS MUSCULAR DYSTROPHY, types 2 and 3; HUTCHINSON-GILFORD PROGERIA SYNDROME; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; Malouf syndrome; Mandibuloacral dysplasia; LMNA-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type.
    DatabaseMESH
    References (5) - MESH
    subject heading

    subject heading

Number of the records: 1  

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