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Results 1 - 10 of 82 for were
  1. Zellweger spectrum disorder 
    ... intermediate, and mild forms of Zellweger spectrum disorder were once thought to be distinct disorders. The severe ... mild form was infantile Refsum disease. These conditions were renamed as a single condition when they were ...
    https://medlineplus.gov/.../condition/zellweger-spectrum-disorder - Genetics
  2. 22q11.2 deletion syndrome 
    ... syndrome are so varied, different groupings of features were once described as separate conditions. Doctors named these ... addition, some children with the 22q11.2 deletion were diagnosed with the autosomal dominant form of Opitz ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  3. What does it mean to have Neanderthal or Denisovan DNA?: MedlinePlus Genetics 
    ... low or undetectable elsewhere in the world. Neanderthals were very early (archaic) humans who lived in Europe ... of early humans who lived in Asia and were distantly related to Neanderthals. (Much less is known ...
    https://medlineplus.gov/.../dtcgenetictesting/neanderthaldna - Genetics
  4. Autism spectrum disorder 
    ... individuals of average or above-average intelligence who were not delayed in their language development. The broader ... may change over time. However, some individuals who were previously diagnosed with one of the subtypes now ...
    https://medlineplus.gov/genetics/condition/autism-spectrum-disorder - Genetics
  5. Klinefelter syndrome 
    ... syndrome affects about 1 in 650 newborns who were assigned male at birth. It is the most ... is a sex chromosome disorder in individuals who were assigned male at birth that results from the ...
    https://medlineplus.gov/genetics/condition/klinefelter-syndrome - Genetics
  6. Pol III-related leukodystrophy 
    ... and symptoms. These varied combinations of clinical features were originally described as separate disorders. Affected individuals may ... of the corpus callosum (HCAHC). Because these disorders were later found to have the same genetic cause, ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  7. POLR3B gene 
    ... and symptoms. These varied combinations of clinical features were originally described as separate disorders. Affected individuals may ... of the corpus callosum (HCAHC). Because these disorders were later found to have the same genetic cause, ...
    https://medlineplus.gov/genetics/gene/polr3b - Genetics
  8. Ehlers-Danlos syndrome 
    ... ways. Originally, 11 forms of Ehlers-Danlos syndrome were named using Roman numerals to indicate the types ( ... include rare forms of Ehlers-Danlos syndrome that were identified more recently. The 2017 classification describes 13 ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  9. L1 syndrome 
    ... adulthood.The conditions that make up L1 syndrome were once thought to be distinct disorders, but since they were found to share a genetic cause, they are ...
    https://medlineplus.gov/genetics/condition/l1-syndrome - Genetics
  10. MYH9-related disorder 
    ... these disorders involved thrombocytopenia and enlarged platelets and were distinguished by some combination of hearing loss, renal ... conditions all had the same genetic cause, they were combined and renamed MYH9-related disorder. The incidence ...
    https://medlineplus.gov/genetics/condition/myh9-related-disorder - Genetics
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