distinction between diseases and phenotypes #2598
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Is this term equivalent to https://hpo.jax.org/app/browse/term/HP:0031576 ? Based on the names and cross-references, I'm not sure how to map this concept for MedGen. UMLS has different identifiers for the HPO term and the OMIM presentation, and the names/synonyms used by the various groups seems to be variably interchangeable... For additional X-refs: GARD 4046 treats Oculomaxillofacial dystosis as equivalent to : " Richieri Costa Gorlin syndrome; Oculomaxillofacial dysplasia with oblique facial clefts; Oblique facial clefts" https://rarediseases.info.nih.gov/diseases/4046/index So perhaps the name "Tessier number 4..." should not be the preferred name on this term, at a minimum, to clarify the clinical presentation as a whole is not equivalent to the precise presentation in the HPO term? |
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This again gets to the distinction between diseases and phenotypes. If a person has a tessier type 4 cleft as their only clinical problem, it is possible to treat it as a disease. On the other had, various kinds of clefts can be observed as features of other diseases. |
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see also: #86 |
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see also #559 |
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another example: #501 |
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These are all excellent examples of the problem with phenotypic feature (which belongs in HPO) and a diagnosis (which belongs in Mondo). The problem becomes even more complicated when a diagnosis is a feature of a disease (e.g. diabetes as part of MELAS (mitochondrial encephalopathy lactic acidosis and stroke). The Discitis example is weird: it is an inflammation of the disc which could be a feature or a diagnosis, especially a diagnosis if the etiology is infection. I think that all of this is/will be very hard. The Tessier type 4 cleft is the description of the cleft. It is definitely a feature and probably of the syndrome, but it sounds like in some people the cleft is the extent of the syndrome... |
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Hello, |
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This is an example use case
The sub-classification of MONDO_0010850 Tessier number 4 facial cleft as a subclass of MONDO_0015824 Oculomaxillofacial dysostosis seems incorrect (although I can't identify the cause - the xref of orphanet_141258 to OMIM_600251 seems okay.
What action should I take here? Should I just remove the parent class assertion in Protege and make a pull request?
Thanks!
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