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• 08:10, 6 April 2022 Homo sapiens:Cholesterol synthesis disorders‎ (Modified title)
• 08:09, 6 April 2022 Homo sapiens:Alstrom syndrome‎ (connected unconnected lines)
• 08:07, 6 April 2022 Homo sapiens:Alstrom syndrome‎ (Ontology Term : 'disease pathway' added !)
• 08:06, 6 April 2022 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis‎ (Ontology Term : 'disease pathway' added !)
• 12:59, 28 March 2022 Homo sapiens:Dravet syndrome‎ (Corrected references)
• 12:16, 28 March 2022 Homo sapiens:Dravet syndrome‎ (Ontology Term : 'neuron' added !)
• 12:16, 28 March 2022 Homo sapiens:Dravet syndrome‎ (Ontology Term : 'disease pathway' added !)
• 12:16, 28 March 2022 Homo sapiens:Dravet syndrome‎ (Ontology Term : 'Dravet syndrome' added !)
• 12:15, 13 December 2021 Homo sapiens:Spina bifida‎ (reference check)
• 08:38, 7 December 2021 Homo sapiens:Spina bifida‎ (Ontology Term : 'folate metabolic pathway' added !)
• 14:06, 30 November 2021 Homo sapiens:Inclusion body myositis‎ (added new pathway)
• 13:48, 30 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis‎ (expert curation workshop updates)
• 09:41, 30 November 2021 Homo sapiens:Serine metabolism‎ (boxed pathway node) (top)
• 09:39, 30 November 2021 Homo sapiens:Riboflavin and CoQ disorders‎ (boxed pathway node)
• 09:37, 30 November 2021 Homo sapiens:Ethylmalonic encephalopathy‎ (fixed graphical clash)
• 09:35, 30 November 2021 Homo sapiens:GABA metabolism (aka GHB)‎ (boxed pathway node)
• 09:34, 30 November 2021 Homo sapiens:Proline and hydroxyproline pathways‎ (boxed pathway node)
• 09:33, 30 November 2021 Homo sapiens:Glycine metabolism, including IMDs‎ (boxed pathway nodes)
• 09:31, 30 November 2021 Homo sapiens:Kisspeptin/kisspeptin receptor system in the ovary‎ (boxed pathway nodes)
• 09:29, 30 November 2021 Homo sapiens:Oxysterols derived from cholesterol‎ (boxed pathway node)
• 09:27, 30 November 2021 Homo sapiens:Krebs cycle disorders‎ (boxed pathway node)
• 09:26, 30 November 2021 Homo sapiens:Thiamine metabolic pathways‎ (boxed pathway nodes)
• 09:24, 30 November 2021 Homo sapiens:Vitamin B12 disorders‎ (small graphical change in pathway node)
• 09:21, 30 November 2021 Homo sapiens:MTHFR deficiency‎ (boxed pathway nodes)
• 09:20, 30 November 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (boxed pathway nodes)
• 09:18, 30 November 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (boxed pathway node)
• 09:16, 30 November 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine‎ (boxed pathway node)
• 09:13, 30 November 2021 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism‎ (boxed pathway nodes)
• 09:12, 30 November 2021 Homo sapiens:Thyroid hormones production and peripheral downstream signaling effects‎ (boxed pathway nodes)
• 09:09, 30 November 2021 Homo sapiens:Pyrimidine metabolism and related diseases‎ (boxed pathway nodes)
• 09:08, 30 November 2021 Homo sapiens:Purine metabolism and related disorders‎ (boxed pathway node)
• 09:06, 30 November 2021 Homo sapiens:Overlap between signal transduction pathways contributing to LMNA laminopathies‎ (small graphical change, boxed pathway nodes)
• 09:02, 30 November 2021 Homo sapiens:Influence of laminopathies on Wnt signaling‎ (small graphical change, boxed pathway nodes)
• 08:59, 30 November 2021 Homo sapiens:Lamin A processing pathway‎ (boxed pathway node)
• 08:56, 30 November 2021 Homo sapiens:Joubert syndrome‎ (boxed pathway nodes)
• 08:52, 30 November 2021 Homo sapiens:Hippo signaling regulation‎ (boxed pathway nodes)
• 08:51, 30 November 2021 Homo sapiens:Degradation pathway of sphingolipids, including diseases‎ (small graphical change)
• 08:49, 30 November 2021 Homo sapiens:Urea cycle and associated pathways‎ (small graphical change: pathway nodes got rounded rectangles)
• 08:44, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 3‎ (small graphical change)
• 08:42, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 2‎ (fixed weird characters in literature list)
• 08:39, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 1‎ (small layout change)
• 08:37, 30 November 2021 Homo sapiens:Acquired partial lipodystrophy / Barraquer-Simons syndrome‎ (small graphical change)
• 08:34, 30 November 2021 Homo sapiens:Kallmann syndrome‎ (Connected unconnected lines)
• 10:07, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis‎ (Ontology Term : 'inclusion body myositis' added !)
• 10:06, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis‎ (converted protein to metabolite)
• 13:13, 11 October 2021 Homo sapiens:22q11.2 copy number variation syndrome‎ (Reverted to version '11:20, 17 September 2021' by <a href="/index.php/User:Fehrhart" title="User:Fehrhart">Fehrhart</a>)
• 11:20, 17 September 2021 Homo sapiens:22q11.2 copy number variation syndrome‎ (Update HIST1H4A for H4C1)
• 09:24, 17 September 2021 Homo sapiens:Male infertility‎ (Updated SEPT12 label to SEPTIN12) (top)
• 09:07, 17 September 2021 Homo sapiens:Parkinson's disease pathway‎ (Updated SEPT5 to SEPTIN5 label)
• 09:07, 17 September 2021 Homo sapiens:Parkin-ubiquitin proteasomal system pathway‎ (Updated SEPT5 to SEPTIN5 label)

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