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[Merge]MONDO:0957115 Neurological muscular channelopathy due to a genetic ryanodine receptor defect" and MONDO:0100150 "RYR1-related myopathy" #8531

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katiermullen opened this issue Jan 5, 2025 · 0 comments

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merge

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katiermullen commented Jan 5, 2025

Mondo term (ID and Label)
MONDO:0957115 Neurological muscular channelopathy due to a genetic ryanodine receptor defect"

Reason for deprecation
In discussions with @galyea123, Neurological muscular channelopathy due to a genetic ryanodine receptor defect ORPHA:98742 appears to be a grouping term and potential duplicate with MONDO:0100150 "RYR1-related myopathy." Needs further confirmation prior to proceeding with merge.

Term to be merged with

MONDO:0100150 "RYR1-related myopathy"

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katiermullen added the merge label

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