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Fraserov syndróm

  1. Subject h.Fraserov syndróm
    Subject h.Fraser Syndrome
    Scope note in EnglishRare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and nose are common. Mutations on FRAS1 and FREM2 are associated with the syndrome.
    See also reference (FX) in Slovak Frasierov syndróm
    See also reference (FX) in English Frasier Syndrome
    Links (1) - MeSH descriptor
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Number of the records: 1  

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