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- Status: Open.#10547 In monarch-initiative/mondo;
- Status: Open.#10545 In monarch-initiative/mondo;
[Merge] MONDO:0018832 'HTRA1-related autosomal dominant cerebral small vessel disease' with MONDO:0014768
on listAdded to the obosletion or merge candidate list.Added to the obosletion or merge candidate list.Status: Open.#10538 In monarch-initiative/mondo;TMX2 disease association - relabel term, add definition
user requestA request from an external userA request from an external userStatus: Open.#10535 In monarch-initiative/mondo;DYNC1H1 disease association - relabel term
user requestA request from an external userA request from an external userStatus: Open.#10533 In monarch-initiative/mondo;PRUNE1 Disease association - rename, keep definition
user requestA request from an external userA request from an external userStatus: Open.#10531 In monarch-initiative/mondo;- Status: Open.#10532 In monarch-initiative/mondo;
MONDO:0034146 and MONDO:0032733 are the same disease (GLS repeat-expansion glutaminase deficiency) — merge
on listAdded to the obosletion or merge candidate list.Added to the obosletion or merge candidate list.Status: Open.#10525 In monarch-initiative/mondo;- Status: Open.#10524 In monarch-initiative/mondo;
- Status: Open.#10522 In monarch-initiative/mondo;
Request for new term: FBN1-related geleophysic and acromelic dysplasia
user requestA request from an external userA request from an external userStatus: Open.#10520 In monarch-initiative/mondo;- Status: Open.#10513 In monarch-initiative/mondo;