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402 Open 3,209 Closed
402 Open 3,209 Closed
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Issues list

Incorrect names for some eponymous diseases bug
#8294 opened Nov 1, 2024 by AleksZakirov
Request for new synonym [RYR1-related myopathy] synonym
#8293 opened Oct 30, 2024 by galyea123
TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations/TP63 New term request
#8292 opened Oct 30, 2024 by eedoh01
Add QC check - class with excluded_subClassOf value does not also have a subClassOf statement
#8290 opened Oct 30, 2024 by twhetzel
1
Update ODK to version 1.5.3
#8288 opened Oct 29, 2024 by twhetzel
1
@twhetzel
[Merge] myoclonic-astatic epilepsy blocked Something needs to be done before work can proceed epilepsy merge workshop
#8287 opened Oct 29, 2024 by nicolevasilevsky
@nicolevasilevsky
Multiple gene associations represented as EquivalentTo
#8276 opened Oct 26, 2024 by twhetzel
Mismatch between the gene symbol used in the SubClassOf restriction vs. the EquivalentTo restriction
#8275 opened Oct 26, 2024 by twhetzel
[Revise subclass] 'developmental and epileptic encephalopathy' Revise subclass
#8274 opened Oct 25, 2024 by nicolevasilevsky
Add Levy-Yeboa syndrome as a synonym for secretory diarrhea, myopathy, and deafness synonym
#8272 opened Oct 24, 2024 by galyea123
Review Design Patterns for neoplasm located in cells
#8271 opened Oct 23, 2024 by twhetzel
Update MEMORY_JAVA setting in run.sh tech issue requiring work from the technical team
#8267 opened Oct 23, 2024 by twhetzel
@twhetzel
X-linked syndromic complex neurodevelopmental disorder New term request
#8266 opened Oct 22, 2024 by Jciesielka1
DHX30-related complex neurodevelopmental disorder New term request
#8265 opened Oct 22, 2024 by Jciesielka1
Syn. on MONDO:0016676 recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome bug OMIM question-Orphanet synonym
#8263 opened Oct 22, 2024 by kanems
Familial chylomicronemia syndrome (formerly known as "type 1 hyperlipoproteinemia.") AND familial lipoprotein lipase deficiency
#8259 opened Oct 18, 2024 by galyea123
Review inconsistent synonym scope on MONDO:0007039 'NF2-related schwannomatosis'
#8258 opened Oct 18, 2024 by twhetzel
3 tasks
@twhetzel
[NTR/TFAP2B] New term request
#8256 opened Oct 17, 2024 by elliebroeren
NDUFB11-Related Disorders New term request
#8253 opened Oct 16, 2024 by galyea123
[Revise subclass]MONDO:0014934 'spinocerebellar ataxia, autosomal recessive 24' Revise subclass
#8237 opened Oct 13, 2024 by katiermullen
@katiermullen
Mito GCEP genes user request A request from an external user
#8229 opened Oct 11, 2024 by mccormickem
Review all Mondo terms which are "and/or"
#8228 opened Oct 10, 2024 by sabrinatoro
1
frontotemporal dementia and/or amyotrophic lateral sclerosis user request A request from an external user
#8227 opened Oct 10, 2024 by sabrinatoro
2
[Revise subclass] inflammatory bowel disease 1 MONDO_0009960 too broad? Revise subclass user request A request from an external user
#8226 opened Oct 10, 2024 by Tobi1kenobi
neonatal-onset encephalopathy with rigidity and seizures and neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures epilepsy user request A request from an external user
#8225 opened Oct 9, 2024 by galyea123
@nicolevasilevsky
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