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Results 1 - 3 of 3 for same "syndrome," digenic
  1. Bardet-Biedl syndrome 
    ... among affected individuals, even among members of the same family.Vision loss is one of the major features of Bardet-Biedl syndrome. Loss of vision occurs as the light-sensing ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  2. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Genetic Testing/Reference Desk ... Genetic Testing ... Newborn Screening/Reference Desk ... Newborn Screening ... National Center for Biotechnology Information ... From the National ...
    https://www.ncbi.nlm.nih.gov/books/NBK5191 - External Health Links
  3. Facioscapulohumeral muscular dystrophy 
    ... permissive" chromosome 4.FSHD2 is inherited in a digenic pattern, which means that two independent genetic changes ... Disorders (NORD) ClinicalTrials.gov FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC; FSHD2 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 PubMed de ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics