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Create the page "1,5-anhydro-D-fructose dehydratase" on this wiki! See also the search results found.

• Wanted pages 1-9
  # [[1+1]] # [[1,1,1,2-Tetrafluoroethane]]
  13 KB (948 words) - 14:50, 26 August 2021
• List of rare metabolic disorders
  * '''[[3 Methylcrotonyl-CoA carboxylase 1 deficiency]]''' * '''[[Adenosine monophosphate deaminase 1 deficiency]]'''
  22 KB (2,804 words) - 22:50, 18 September 2019
• Metabolic disorders
  * '''[[Adenosine monophosphate deaminase 1 deficiency]]''' * '''[[Alpha-1 antitrypsin deficiency]]'''
  26 KB (3,173 words) - 19:37, 20 September 2023
• List of diseases (D)
  * [[Dehydratase deficiency]] * [[Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency]]
  13 KB (1,212 words) - 04:31, 4 October 2019
• List of rare diseases-H
  {{Plainlist|indent=1}} * '''[[Heart block progressive familial type 1]]'''
  57 KB (7,147 words) - 03:26, 10 April 2022
• List of rare diseases-D
  {{Plainlist|indent=1}} * '''[[Deficiency of interleukin-1 receptor antagonist]]'''
  45 KB (5,893 words) - 03:15, 10 April 2022
• List of rare nervous system diseases
  * '''[[2q23.1 microdeletion syndrome]]''' * '''[[Adenosine monophosphate deaminase 1 deficiency]]'''
  59 KB (7,384 words) - 08:53, 14 March 2024
• List of human genes
  ....nlm.nih.gov/gene/ABCA1 ABCA1]''': ATP binding cassette subfamily A member 1 ....nlm.nih.gov/gene/ABCD1 ABCD1]''': ATP binding cassette subfamily D member 1
  121 KB (20,808 words) - 02:03, 14 March 2024
• Skin diseases
  * '''[[Aminolevulinate dehydratase deficiency porphyria]]''' * '''[[Cutis laxa, autosomal recessive type 1]]'''
  26 KB (3,264 words) - 07:04, 23 June 2020
• List of rare skin diseases
  * '''[[Aminolevulinate dehydratase deficiency porphyria]]''' * '''[[Cutis laxa, autosomal recessive type 1]]'''
  26 KB (3,281 words) - 22:40, 18 September 2019
• Diseases-and-disorders-A
  * '''[[2p15-16.1 microdeletion syndrome]]''' * '''[[4-Nitroquinoline 1-oxide]]'''
  27 KB (3,632 words) - 18:05, 1 October 2019
• Wanted pages D
  # [[Decoy receptor 1]] # [[Delta-aminolevulinic acid dehydratase]]
  32 KB (2,968 words) - 14:57, 26 August 2021
• MeSH L
  * '''[[L-Serine Dehydratase]]''' * '''[[Large Neutral Amino Acid-Transporter 1]]'''
  31 KB (4,062 words) - 03:45, 10 March 2024
• List of rare diseases-T
  {{Plainlist|indent=1}} * '''[[TCO 1]]'''
  30 KB (4,018 words) - 03:37, 10 April 2022
• Congenital and genetic diseases
  * '''[[1q21.1 microdeletion syndrome]]''' * '''[[2p15p16.1 microdeletion syndrome]]'''
  138 KB (16,857 words) - 05:28, 19 March 2024
• List of rare congenital and genetic diseases
  * '''[[1q21.1 microdeletion syndrome]]''' * '''[[2p15p16.1 microdeletion syndrome]]'''
  137 KB (17,056 words) - 17:46, 19 March 2024
• MeSH T
  * '''[[T Cell Transcription Factor 1]]''' * '''[[T-Cell Acute Lymphocytic Leukemia Protein 1]]'''
  46 KB (5,950 words) - 03:46, 10 March 2024
• List of rare diseases-A
  {{Plainlist|indent=1}} * '''[[Acrocephalo-syndactyly type 1]]'''
  99 KB (12,050 words) - 02:28, 10 April 2022
• MeSH P
  * '''[[Parainfluenza Virus 1, Human]]''' * '''[[Patched-1 Receptor]]'''
  94 KB (11,917 words) - 03:45, 10 March 2024
• List of rare diseases-P
  {{Plainlist|indent=1}} * '''[[PAI-1 deficiency]]'''
  76 KB (9,827 words) - 03:35, 10 April 2022

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