Changes related to "Portal:RareDisease"

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< Portal:RareDisease

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18 June 2019

• Homo sapiens:Pyrimidine metabolism and related diseases‎; 17:43 . . (+4,036) . . IreneHemel (Talk | contribs) (Added legend)
• Homo sapiens:Fragile X Syndrome ‎; 08:08 . . (+280) . . Fehrhart (Talk | contribs) (Connected unconnected lines)
• Homo sapiens:NBIA subtypes pathway‎; 06:57 . . (+644) . . GMKeulen (Talk | contribs) (Changed background color of lipid metabolism.)

13 June 2019

• Homo sapiens:NBIA subtypes pathway‎; 10:32 . . (+692) . . GMKeulen (Talk | contribs) (Added pathway node.)
• Homo sapiens:NBIA subtypes pathway‎; 10:16 . . (-51) . . GMKeulen (Talk | contribs) (Added CheBI identifiers, changed mim-interactions to arrows.)
• Homo sapiens:Purine metabolism‎; 07:31 . . (0) . . Josienlandman (Talk | contribs) (Corrected the identifier for AICA-riboside)