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- VSCode Version: Anything Has the community at large expressed interest in this functionality? I.e. has it gathered more than 10 up-votes or more than 10 comments?
Well no. The majority of these …
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```
[Term]
id: MONDO:0035087
name: acute myeloid leukemia with t(9;22)(q34.1;q11.2)
subset: ordo_disease
is_a: MONDO:0000001 {source="Orphanet:585867"} ! disease or disorder
is_a: MONDO:0020078 …
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Preferred term label: NAA10-related syndrome
Synonyms/Other Disease Assertions: Odgen Syndrome, Lenz Microphthalmia Syndrome, Autism Spectrum Disorder, Intellectual Disability
Definition (fr…
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With the release of EFO 3.23.0, there will be new phenotype data that we can integrate into the Platform to enrich the disease index and display on the disease profile page
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**(1) Use more formatting to help chunk out the information and make it easier to digest.**
This is especially important for 2.2 (Background), which contains essential information but is hard to get…
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**Preferred term label:**
Impaired ability to shift
**Synonyms**
Sticky behavior
Inflexible behavior - broad
Impaired set shifting
**Definition (free text, please give PubMed ID)**
A behavi…
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It would be nice to provide the parameter `include_children` to the `/rest/trait/all` endpoint.
Right now what I do, as an alternative, is to get all EFO identifiers with `/rest/trait/all` first, …
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As one can see for the following Item, Senior Theses Items imported from submissions for certificate programs are members of multiple collections, one being the departmental collection, the other bein…
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We have a request from the Monogenic Diabetes GCEP to change a current MonDO ID for the gene INS for autosomal recessive inheritance.
The UUID for the curation is: https://curation.clinicalgenome.…
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Hi,
for Uniprot release 2021-01 we require the following MONDO terms for mapping:
Not sure how the omim ingests work now on your end, so thought I'd raise this request. I have attached the DI de…