Colleagues in our Computer Science department are developing a tool which identifies genes and medical terms taken from MeSH headings and its hierarchy (category C). I suppose that this in some way could be described as identifying co-morbidities and the responsible genes, but there are other things that they're also trying to solve.
I suggested that they also try to link the disease terms to symptoms whether they be external (eg, skin rash), invasive (eg, red blood cell count) or clinical (eg, results of a culture). However, no one present knew of a digital database linking symptoms to MeSH disease headings (category C), or anything similar.
Thus, we'd be grateful for any pointers or advice on this topic.
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Larry_Parnell
Not exactly a database solution, but a set of terminologies related to clinical symptoms / clinical procedures / classification of diseases are routinely used in biomedical informatics projects like the one you explained.
These terminologies were already mapped or can be mapped to MeSH terms.
See manuscript describing mapping of SNOMED-CT to MeSH here and ICD-9 to MeSH here.
Thanks, Khader. I thought that you would have something to contribute on this topic.
You might also take a look at the Unified Medical Language System here, which includes MeSH. Often it also includes additional terms that are not found in MeSH.
Depending on your phenotypes, the Human Phenotype Ontology Website here may be useful.
Thank you, Alex. These are good points to pass to my colleagues.
I am cross posting from my reply from another post. Have a look at the Human symptoms–disease network. All the disease-symptoms relationships identified from text mining on Pubmed meta data and mapped to MeSH are in the supplementary data set 3.
I have been working on a disease symptom database from scratch, inputting data directly from primary references. My project is available for viewing here. I have been thinking about making an API if there is enough interest... Comments / suggestions welcome!
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