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Remove OMIM gene mentions from Mondo xrefs / provenance
#7983
opened Jul 21, 2024 by
matentzn
4 tasks
SPATA5L1-related complex neurodevelopmental disorder with motor features and hearing loss
relabel term
#7975
opened Jul 18, 2024 by
icordovaG
split term or relabel?: infantile spasms (currently synonym of West syndrome
epilepsy
split
requests for term splits
synonym
#7969
opened Jul 16, 2024 by
nicolevasilevsky
weiss-kruszka syndrome (MONDO:0032836)- Relabel Weiss-Kruszka Syndrome
relabel term
#7965
opened Jul 15, 2024 by
madysoncbrown
[Revise subclass] Noonan syndrome is not always a cardiogenetic syndrome
Revise subclass
#7959
opened Jul 13, 2024 by
pnrobinson
[Obsolete] MONDO:0015422 orofaciodigital syndrome type 13
obsolete
This includes both obsolete and merge requests
#7956
opened Jul 13, 2024 by
twhetzel
RTN4IP1-related optic atrophy with or without neurological features
New term request
#7951
opened Jul 12, 2024 by
poppies700
[Revise subclass] Parkinson is not necessarily herreditary
Revise subclass
#7947
opened Jul 11, 2024 by
pnrobinson
[Revise subclass] Cutis laxa is not necessarily congenital entropion
bug
Revise subclass
#7946
opened Jul 11, 2024 by
pnrobinson
[Revise subclass] neurodevelopmental disorder
bug
Revise subclass
#7943
opened Jul 11, 2024 by
pnrobinson
Bulk request for new gene related syndrome terms from ClinGen Retina GCEP
New term request
#7923
opened Jul 5, 2024 by
wchankey
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