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Results 61 - 70 of 103 for Abnormal embryonic development
  1. STING-associated vasculopathy with onset in infancy 
    ... reproductive cells (eggs or sperm) or in early embryonic development. These cases occur in people with no history ...
    https://medlineplus.gov/...ciated-vasculopathy-with-onset-in-infancy - Genetics
  2. Angelman syndrome 
    ... reproductive cells (eggs and sperm) or in early embryonic development. Affected people typically have no history of the ...
    https://medlineplus.gov/genetics/condition/angelman-syndrome - Genetics
  3. 47,XYY syndrome 
    ... a random event during cell division in early embryonic development. As a result, some of an affected person' ...
    https://medlineplus.gov/genetics/condition/47xyy-syndrome - Genetics
  4. Crouzon syndrome 
    ... signals immature cells to become bone cells during embryonic development. Mutations in the FGFR2 gene are thought to ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  5. Pfeiffer syndrome 
    ... signal immature cells to become bone cells during embryonic development. A mutation in either the FGFR1 or FGFR2 ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  6. Primary macronodular adrenal hyperplasia 
    ... gene mutation is believed to occur early in embryonic development. Cells with the mutated GNAS gene can be ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics
  7. MECP2 duplication syndrome 
    ... to a process called X-inactivation. Early in embryonic development in females, one of the two X chromosomes ...
    https://medlineplus.gov/.../condition/mecp2-duplication-syndrome - Genetics
  8. Sporadic hemiplegic migraine 
    ... de novo) mutations that likely occur during early embryonic development, some affected individuals inherit the genetic change that ...
    https://medlineplus.gov/.../condition/sporadic-hemiplegic-migraine - Genetics
  9. Spondyloepiphyseal dysplasia with marked metaphyseal changes 
    ... an affected individual's parent or during early embryonic development. These affected individuals typically have no history of ...
    https://medlineplus.gov/...dysplasia-with-marked-metaphyseal-changes - Genetics
  10. Shwachman-Diamond syndrome 
    ... or sperm) in the parent or during early embryonic development.Rarely, the condition is inherited in an autosomal ...
    https://medlineplus.gov/.../condition/shwachman-diamond-syndrome - Genetics
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