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**Mondo term (ID and Label):**
MONDO:0957426 autosomal recessive hyper-IgE syndrome
**Suggested new label:**
If this is, indeed an exact match to Orphanet 641368 , then the pref name should be Au…
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**Mondo term (ID and Label)**
MONDO:0957319, pseudohypoaldosteronism, type I
**Reason for deprecation**
I think these may be the same? The Orphanet mappings only partially overlap with the OMIM P…
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One of Translator's automated tests is for MONDO:0005799 (hookworm infectious disease).
BTE may be returning no results from this test because [NodeNorm doesn't find any equivalent IDs in other na…
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**Mondo term (ID and Label)**
MONDO:0035383 FOXG1 syndrome
**Reason for deprecation**
GeneReviews uses FOXG1 syndrome as their preferred name for this chapter: https://www.ncbi.nlm.nih.gov/books/…
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Please process the following downloaded protein datasets for 2.6. The EBI and NCBI datasets include the new organism Arabidopsis.
/data/projects/glygen/downloads/genomics_england/current
/data/pro…
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### Label
congenital myasthenic syndrome 4
### Synonyms
_No response_
### Synonym type
None
### Definition
Any congenital myasthenic syndrome in which the cause of the disease is a mutation in …
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## Overview
This is causing errors when Joe runs `build-mondo-ingest`. There are several places ot remove.
Joe has many more notes in Workflowy.
Why isn't Nico having this problem? Is it becaus…
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**Mondo term (ID and Label)**
Parkinson disease 13, autosomal dominant, susceptibility to (MONDO:0012466)
Any young-onset Parkinson disease in which the cause of the disease is a mutation in the H…
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**Mondo term (ID and Label):**
MONDO:0005279 (pulmonary embolism)
**Xref that should be fixed (ID and label):**
equivalentTo: ICD10 I26: (Pulmonary embolism )
**Your nano-attribution (ORCID)**…
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https://site.imondo.cn/article/#/ruadwn