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Results 1 - 10 of 58 for Diabetes
  1. MT-TE gene 
    ... a small number of people with maternally inherited diabetes and deafness (MIDD). People with this condition have diabetes and sometimes hearing loss, particularly of high tones. ...
    https://medlineplus.gov/genetics/gene/mt-te - Genetics
  2. PLAGL1 gene 
    ... a mechanism called methylation. 6q24-related transient neonatal diabetes mellitus, a type of diabetes that occurs in infants, is caused by the ... percent of cases of 6q24-related transient neonatal diabetes mellitus are caused by a genetic change known ...
    https://medlineplus.gov/genetics/gene/plagl1 - Genetics
  3. ZFP57 gene 
    ... percent of cases of 6q24-related transient neonatal diabetes mellitus, a type of diabetes that occurs in infants. This disorder results from ... in the impaired blood glucose control associated with diabetes mellitus.Because HIL resulting from ZFP57 gene mutations ...
    https://medlineplus.gov/genetics/gene/zfp57 - Genetics
  4. ABCC8 gene 
    ... have been identified in people with permanent neonatal diabetes mellitus. Individuals with this condition often have a ... life.ABCC8 gene mutations that cause permanent neonatal diabetes mellitus change single amino acids in the protein ...
    https://medlineplus.gov/genetics/gene/abcc8 - Genetics
  5. GCK gene 
    ... Mutations in the GCK gene cause maturity-onset diabetes of the young (MODY), which is a group ... abnormally high blood glucose levels. This form of diabetes usually begins before age 30. GCK gene mutations ...
    https://medlineplus.gov/genetics/gene/gck - Genetics
  6. HNF1B gene 
    ... Mutations in the HNF1B gene cause maturity-onset diabetes of the young (MODY). MODY is a group ... type of MODY known as renal cysts and diabetes (RCAD) syndrome (also known as HNF1B-MODY or ...
    https://medlineplus.gov/genetics/gene/hnf1b - Genetics
  7. KCNJ11 gene 
    ... have been identified in people with permanent neonatal diabetes mellitus. Individuals with this condition often have a ... life.KCNJ11 gene mutations that cause permanent neonatal diabetes mellitus change single amino acids in the protein ...
    https://medlineplus.gov/genetics/gene/kcnj11 - Genetics
  8. INS gene 
    ... have been identified in people with permanent neonatal diabetes mellitus. Individuals with this condition often have a ... life.INS gene mutations that cause permanent neonatal diabetes mellitus change single protein building blocks (amino acids) ...
    https://medlineplus.gov/genetics/gene/ins - Genetics
  9. AVP gene 
    ... and concepts in the diagnosis and management of diabetes insipidus (AVP-deficiency and resistance). J Neuroendocrinol. 2023 ... on PubMed Christensen JH, Rittig S. Familial neurohypophyseal diabetes insipidus--an update. Semin Nephrol. 2006 May;26( ...
    https://medlineplus.gov/genetics/gene/avp - Genetics
  10. HLA-DQB1 gene 
    ... HLA genes affect the risk of type 1 diabetes. Type 1 diabetes is characterized by high levels of blood glucose, ... insulin-producing cells in the pancreas.Type 1 diabetes risk is most increased by two specific combinations ...
    https://medlineplus.gov/genetics/gene/hla-dqb1 - Genetics
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