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Results 1 - 10 of 624 for little syndrome 2
  1. Familial cold autoinflammatory syndrome type 2 
    ... may influence the severity of familial cold autoinflammatory syndrome type 2, but little is known about how these changes contribute to the condition. NLRP12 In most cases, familial cold autoinflammatory syndrome type 2 is inherited in an autosomal dominant pattern, which ...
    https://medlineplus.gov/...ial-cold-autoinflammatory-syndrome-type-2 - Genetics
  2. NLRP12 gene 
    ... may influence the severity of familial cold autoinflammatory syndrome type 2, but little is known about how these changes contribute to the condition.In some families, individuals with an NLRP12 gene variant may develop ... syndrome type 2 but others with the mutation do not, which ...
    https://medlineplus.gov/genetics/gene/nlrp12 - Genetics
  3. COMT gene 
    ... behavioral problems and mental illness associated with 22q11.2 deletion syndrome. Little is known, however, about the relationship between catechol-O-methyltransferase activity and the specific mental and emotional problems ... 22q11.2 deletion syndrome are much more likely than people without the ...
    https://medlineplus.gov/genetics/gene/comt - Genetics
  4. Interstitial Nephritis (American Academy of Family Physicians)  
    Kidney Diseases/Specifics ... Kidney Diseases ... American Academy of Family Physicians
    https://familydoctor.org/.../interstitial-nephritis/?adfree=true - External Health Links
  5. 16p11.2 deletion syndrome 
    ... more than 25 genes, and in many cases little is known about their function. Researchers are working to determine how the missing genes contribute to the features of 16p11.2 deletion syndrome. chromosome 16 16p11.2 deletion syndrome is considered ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  6. Chromosome 16 
    ... more than 25 genes, and in many cases little is known about their function. Researchers are working to determine how the missing genes contribute to the features of 16p11.2 deletion syndrome, which include delayed development; intellectual disability; and autism ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  7. About Antiphospholipid Syndrome (APS) From the National Institutes of Health (National Human Genome Research Institute)  
    Autoimmune Diseases/Specifics ... Autoimmune Diseases ... National Human Genome Research Institute ... From the National Institutes of Health ... Antiphospholipid Syndrome ...
    https://www.genome.gov/Genetic-Disorders/Antiphospholipid-Syndrome - External Health Links
  8. Luteinizing hormone (LH) blood test 
    ... polycystic ovary syndrome ) During or after menopause Turner syndrome (rare genetic condition in which a female does not have the usual pair of 2 X chromosomes) When the ovaries produce little or no hormones (ovarian hypofunction) In men, a ...
    https://medlineplus.gov/ency/article/003708.htm - Medical Encyclopedia
  9. Cannabis (Marijuana) and Cannabinoids: What You Need To Know From the National Institutes of Health (National Center for Complementary and Integrative Health)  
    Marijuana/Start Here ... Marijuana ... National Center for Complementary and Integrative Health ... Are marijuana and cannabis the same thing? What are cannabinoids? ...
    https://www.nccih.nih.gov/...-and-cannabinoids-what-you-need-to-know - External Health Links
  10. TGFBR2 gene 
    ... Most TGFBR2 gene mutations that cause Loeys-Dietz syndrome change single protein building blocks (amino acids) in TGF-β receptor type 2, resulting in a receptor with little or no function. Although the receptor has severely ...
    https://medlineplus.gov/genetics/gene/tgfbr2 - Genetics
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