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Results 1 - 10 of 534 for 20S -"19,20,22,23-TETRAHYDRO-19-OXO-5H,21H-18,20-ETHANO-12,14-ETHENO-6,10-METHENOBENZ[D]IMIDAZO[4,3-L][1,6,9,13]OXATRIAZACYCLONOADECOSINE-9-CARBONITRILE"
Did you mean 20S -"19,20,22,23-tetra hydro-19-OXO-5H,21H-18,20-than-12,14-then-6,10-METHENOBENZ[D]IMIDAZO[4,3-L][1,6,9,13]OXATRIAZACYCLONOADECOSINE-9-CARBONITRILE"?
  1. 17 alpha-hydroxylase/17,20-lyase deficiency 
    17 alpha(α)-hydroxylase/17,20-lyase deficiency is a condition that affects the function of certain hormone-producing glands called the gonads (ovaries in ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  2. Ring chromosome 20 syndrome 
    Ring chromosome 20 syndrome is a condition that affects the normal development and function of the brain. The most common feature ... also appear to be characteristic of ring chromosome 20 syndrome. These episodes involve confusion and behavioral changes. ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  3. Alagille syndrome 
    ... have small deletions of genetic material on chromosome 20 that include the JAG1 gene. A few people ... column, and certain facial features. JAG1 NOTCH2 chromosome 20 This condition is inherited in an autosomal dominant ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  4. Cone-rod dystrophy 
    ... are known to cause cone-rod dystrophy. Approximately 20 of these genes are associated with the form ... dystrophy 2 Genetic Testing Registry: Cone-rod dystrophy 20 Genetic Testing Registry: Cone-rod dystrophy 3 Genetic ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  5. Amyotrophic lateral sclerosis 
    ... disease progression varies widely among affected individuals.Approximately 20 percent of individuals with ALS also develop FTD. ... Europe. Worldwide, SOD1 gene mutations cause 15 to 20 percent of familial ALS, and TARDBP and FUS ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  6. X-linked dilated cardiomyopathy 
    ... in X-linked dilated cardiomyopathy. Circulation. 1997 May 20;95(10):2344-7. doi: 10.1161/01. ... PS. Dystrophinopathies. 2000 Sep 5 [updated 2022 Jan 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/.../x-linked-dilated-cardiomyopathy - Genetics
  7. Preeclampsia 
    ... any obvious signs of preeclampsia.Between 10 and 20 percent of women with severe preeclampsia develop another ... multiples, being older than 35 or younger than 20, and preexisting health conditions. Socioeconomic status and ethnicity ...
    https://medlineplus.gov/genetics/condition/preeclampsia - Genetics
  8. 9q22.3 microdeletion 
    ... in people with a 9q22.3 microdeletion.About 20 percent of people with a 9q22.3 microdeletion ... be much larger; the largest reported deletion includes 20.5 million base pairs (20.5 Mb). 9q22. ...
    https://medlineplus.gov/genetics/condition/9q223-microdeletion - Genetics
  9. Koolen-de Vries syndrome 
    ... the H2 lineage. This variant is found in 20 percent of people of European and Middle Eastern ... j.ejmg.2010.11.003. Epub 2010 Nov 20. Citation on PubMed Egger JI, Wingbermuhle E, Verhoeven ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  10. Shingles 
    ... This form of shingles, which accounts for about 20 percent of cases, can cause permanent vision impairment. ... can recur in rare cases.In 5 to 20 percent of people with shingles, severe pain continues ...
    https://medlineplus.gov/genetics/condition/shingles - Genetics
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