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• Cybs
  {{PAGENAME}} - human sdhd wild type allele is located in the vicinity of 11q23 and is approximately 33 kb in length. This allele, which encodes succinate
  578 bytes (76 words) - 01:57, 7 April 2024
• T3d
  {{PAGENAME}} - human cd3d wild type allele is located within 11q23 and is approximately 4 kb in length. This allele, which encodes t cell surf
  570 bytes (88 words) - 17:23, 6 April 2024
• ALG9-CDG (CDG-IL)
  .... The disease is caused by loss-of-function mutations in the gene '''ALG9 (11q23)'''.
  970 bytes (116 words) - 10:33, 13 September 2020
• Apolipoprotein A-I
  The gene encoding ApoA-I is located on chromosome 11q23-q24. Mutations in this gene can lead to various phenotypes, including HDL d
  2 KB (320 words) - 18:13, 27 March 2024
• Renal hypomagnesemia 2
  ADPHH is caused by mutations in the '''FXYD2 gene (11q23; mutation p.Gly41Arg)''' which encodes the '''gamma subunit of the Na+/K+-A
  3 KB (339 words) - 10:19, 17 November 2020
• KMT
  ...leukemia. The most common alteration is a translocation between chromosome 11q23, where KMT2A is located, and various other chromosomes. These translocation
  3 KB (466 words) - 08:24, 22 March 2024
• Apolipoprotein A1
  The gene encoding Apolipoprotein A1 is located on chromosome 11q23-q24. Mutations in this gene can lead to various metabolic disorders, includ
  3 KB (425 words) - 07:21, 22 March 2024
• MLL (gene)
  '''MLL''' (Mixed-Lineage Leukemia) is a [[gene]] located on [[chromosome]] 11q23, which plays a critical role in the regulation of [[gene expression]] durin
  3 KB (441 words) - 19:24, 13 April 2024
• KMT2A
  ...own as '''MLL''' (Mixed-Lineage Leukemia), is a gene located on chromosome 11q23 that plays a critical role in the regulation of gene expression through his
  3 KB (437 words) - 08:37, 19 March 2024
• Acute monoblastic leukemia
  ...g '''chromosome 11''', such as t(9;11), affecting the MLL (KMTA2) locus at 11q23; however MLL translocations are also found in other leukemia subtypes. The
  3 KB (437 words) - 02:38, 3 August 2020
• Rosselli–Gulienetti syndrome
  * Zlotogora-Ogur syndrome is caused by mutations in the gene '''PVRL1 (11q23-q24) which encodes nectin-1''', the principal receptor '''used by alpha-her
  5 KB (579 words) - 18:10, 26 May 2021
• Medical-dictionary-0-9
  * [[11q23 anomaly]] * [[11q23 q24]]
  14 KB (1,362 words) - 02:37, 5 November 2023
• ICD-10 Chapter II: Neoplasms
  * '''[[C9260]]''' Acute myeloid leukemia with 11q23-abnormality not having achieved remission * '''[[C9261]]''' Acute myeloid leukemia with 11q23-abnormality in remission
  120 KB (17,396 words) - 03:41, 14 December 2020
• ICD 11 codes page 10
  | XH2S51||- - - - Mixed phenotype acute leukaemia with t(v;11q23); MLL rearranged | XH8GG0||- - - - B lymphoblastic leukaemia/lymphoma with t(v;11q23); MLL rearranged
  182 KB (38,418 words) - 05:24, 14 December 2020
• List of neoplasms
  ...of lymphoblasts that carry a translocation between the mll (kmt2a) gene at 11q23.3 and another gene partner resulting in the production of an mll related fu ...b-lymphoblasts and carries a translocation between the mll (kmt2a) gene at 11q23.3 and another gene partner resulting in the production of an mll related fu
  397 KB (57,458 words) - 17:44, 19 March 2024
• Encyclopedia-of-medicine-B
  *[[B lymphoblastic leukemia/lymphoma with t(v;11q23); mll rearranged]]
  91 KB (9,485 words) - 13:18, 29 August 2022