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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. CYLD cutaneous syndrome 
    ... benign growths called cylindromas, spiradenomas, and trichoepitheliomas. Cylindromas were previously thought to derive from sweat glands, but ... multiple familial trichoepithelioma, and familial cylindromatosis. These conditions were once thought to be distinct disorders but are ...
    https://medlineplus.gov/genetics/condition/cyld-cutaneous-syndrome - Genetics
  5. 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
  6. FA2H gene 
    ... some of the movement problems seen in FAHN were once classified as having a separate disorder called ... resulting in intellectual decline and optic nerve atrophy were said to have a disorder called FA2H-related ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  7. Fatty acid hydroxylase-associated neurodegeneration 
    ... some of the movement problems seen in FAHN were once classified as having a separate disorder called ... resulting in intellectual decline and optic nerve atrophy were said to have a disorder called FA2H-related ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  8. Hidradenitis suppurativa 
    ... rare condition because only the most severe cases were reported. However, recent studies have shown that the ... role in causing the disease. Other factors that were mistakenly thought to be associated with this condition ...
    https://medlineplus.gov/genetics/condition/hidradenitis-suppurativa - Genetics
  9. 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
  10. Langerhans cell histiocytosis 
    ... individuals. Certain presentations or forms of the disorder were formerly considered to be separate diseases. Older names that were sometimes used for forms of Langerhans cell histiocytosis ...
    https://medlineplus.gov/.../condition/langerhans-cell-histiocytosis - Genetics
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