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Results 1 - 10 of 67 for "X-linked" dominant inheritance
  1. If a genetic disorder runs in my family, what are the chances that my children will have the condition?: MedlinePlus ... 
    ... child who is a carrier is 50 percent. X-linked dominant inheritance: The chance of passing on an X-linked ... Therefore, the sons of a man with an X-linked dominant disorder will not be affected, but all of his daughters ...
    https://medlineplus.gov/.../understanding/inheritance/riskassessment - Genetics
  2. Hereditary hypophosphatemic rickets 
    ... X-linked hypophosphatemic rickets (XLH). It has an X-linked dominant pattern of inheritance. X-linked recessive, autosomal dominant, and autosomal recessive ...
    https://medlineplus.gov/.../hereditary-hypophosphatemic-rickets - Genetics
  3. X-linked acrogigantism 
    ... GHRH. GPR101 x chromosome X-LAG follows an X-linked dominant inheritance pattern. The gene associated with this condition is ...
    https://medlineplus.gov/genetics/condition/x-linked-acrogigantism - Genetics
  4. BCOR gene 
    ... have two X chromosomes). OFCD syndrome has an X-linked dominant inheritance pattern, which means that one altered copy of ...
    https://medlineplus.gov/genetics/gene/bcor - Genetics
  5. Oculofaciocardiodental syndrome 
    ... X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance. Am J Med Genet A. 2003 Dec 15; ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics
  6. Rett syndrome 
    ... variants caused by MECP2 gene mutations have an X-linked dominant pattern of inheritance. A condition is considered X-linked if the mutated gene that causes the disorder ...
    https://medlineplus.gov/genetics/condition/rett-syndrome - Genetics
  7. Cornelia de Lange syndrome 
    ... HDAC8 or SMC1A gene, the condition has an X-linked dominant pattern of inheritance. A condition is considered X-linked if the altered gene that causes the disorder ...
    https://medlineplus.gov/.../condition/cornelia-de-lange-syndrome - Genetics
  8. Porphyria 
    ... mutations in the ALAS2 gene, it has an X-linked dominant pattern of inheritance. The ALAS2 gene is located on the X ... gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or ... or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/porphyria -
  9. Nearsightedness 
    ... can follow an autosomal dominant, autosomal recessive, or X-linked inheritance pattern. In autosomal dominant inheritance, one copy of an altered gene in ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  10. Cutis laxa 
    ... can have an autosomal dominant, autosomal recessive, or X-linked recessive pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
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