Changes related to "Portal:RareDisease"

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< Portal:RareDisease

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24 October 2020

• Homo sapiens:Classical pathway of steroidogenesis, including diseases‎; 09:13 . . (-1) . . DeSl (Talk | contribs) (Updating ID for cortisol to avoid duplicate mappings)

23 October 2020

• Homo sapiens:16p11.2 proximal deletion syndrome‎; 07:25 . . (+2) . . Egonw (Talk | contribs) (Replaced secondary ChEBI identifiers)

22 October 2020

• Homo sapiens:16p11.2 proximal deletion syndrome‎; 15:22 . . (+9,102) . . Fehrhart (Talk | contribs) (work in progress)
• Homo sapiens:16p11.2 proximal deletion syndrome‎; 15:03 . . (+18,914) . . Fehrhart (Talk | contribs) (work in progress )
• Homo sapiens:16p11.2 proximal deletion syndrome‎; 09:01 . . (+3,357) . . Fehrhart (Talk | contribs) (work in progress)

20 October 2020

• Homo sapiens:16p11.2 proximal deletion syndrome‎; 10:24 . . (+7,278) . . Fehrhart (Talk | contribs) (work in progress)
• Homo sapiens:7q11.23 copy number variation syndrome‎; 10:08 . . (+148) . . Fehrhart (Talk | contribs) (converted legend to graphical line)
• Homo sapiens:16p11.2 proximal deletion syndrome‎; 10:07 . . (+8,998) . . Fehrhart (Talk | contribs) (work in progress)
• Homo sapiens:16p11.2 proximal deletion syndrome‎; 09:36 . . (+11,658) . . Fehrhart (Talk | contribs) (work in progress )