Changes related to "Portal:RareDisease"

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< Portal:RareDisease

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16 August 2019

• Homo sapiens:Cerebral Organic Acidurias, including diseases‎; 12:09 . . (+294) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:Tyrosine Metabolism‎; 12:09 . . (+2) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:Neurotransmitter Disorders‎; 12:09 . . (+4) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:The alternative pathway of fetal androgen synthesis‎; 12:06 . . (+405) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:Viral Acute Myocarditis‎; 12:04 . . (+6) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:Molybdenum cofactor (Moco) biosynthesis‎; 12:04 . . (+2) . . MaintBot (Talk | contribs) (HMDB identifier normalization)
• Homo sapiens:Amyotrophic lateral sclerosis (ALS)‎; 04:52 . . (+38) . . Khanspers (Talk | contribs) (Modified description)
• Homo sapiens:Alzheimers Disease‎; 04:50 . . (+38) . . Khanspers (Talk | contribs) (Modified description)

15 August 2019

• Homo sapiens:Purine metabolism‎; 22:47 . . (-719) . . Khanspers (Talk | contribs) (Modified description)
• Homo sapiens:Prion disease pathway‎; 19:49 . . (+104) . . Khanspers (Talk | contribs) (Modified description)
• Homo sapiens:Parkinsons Disease Pathway‎; 19:42 . . (-234) . . Khanspers (Talk | contribs) (Modified description)