MONDO:0022413 Albright-like syndrome

[kanems]

MONDO:0022413 Albright-like syndrome Points to a link in GARD that is no longer active. There is no disease definition and very little information on OLS about phenotypes... I note Subclass of ... disease shares features ofsomepolyostotic fibrous dysplasia

And then string similarity suggests maybe this could be merged with MONDO:0010886 2q37 microdeletion syndrome (SYN from OMIM of "Albright hereditary osteodystrophy-like syndrome") Or maybe obsolete this Albright-like syndrome concept with a suggested alternate of the 2q37 microdeletion? I am not sure, but I would appreciate if there could be some review of MONDO:0022413 . Right now MedGen can't map it to any CUIs in UMLS or other sources, so we're not displaying it publicly.

[sagehrke]

Dear @kanems, Thank you for reaching out to the Mondo Disease Ontology, part of the Monarch Initiative!

We have received your ticket and will review it as soon as possible.

If you have any additional information or updates relevant to your inquiry, please add them in a comment on this ticket. Your input is valuable in helping us understand and resolve the issue effectively.

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Sincerely, The Mondo Team

[twhetzel]

NOTE: this term is on the obsoletion candidate list following this issue: https://github.com/monarch-initiative/mondo/issues/7700

Is it ok then to close this ticket?

[sabrinatoro]

I agree, I wasn't able to find information about "Albright-like syndrome". In addition, there is no source for the SubClass annotation "'disease shares features of' some 'polyostotic fibrous dysplasia'"

I will obsolete the term and add a "consider" annotation for the following two diseases: MONDO:0018919 - 'McCune-Albright syndrome' MONDO:0010886 - '2q37 microdeletion syndrome'