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Mondo Disease Ontology
http://obofoundry.org/ontology/mondo
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[Revise subclass] Parkinson disease 13, autosomal dominant, susceptibility to (MONDO:0012466) #7827

Open ValWood opened 5 months ago

ValWood commented 5 months ago

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 HTRA2 gene.

Suggested revision and reasons

add young-onset Parkinson disease (MONDO:0017279)

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sagehrke commented 5 months ago

Dear @ValWood, 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.

Thank you for your patience and for your contributions to Mondo!

Sincerely, The Mondo Team

twhetzel commented 1 week ago

Hi @ValWood - is the request to add 'young-onset Parkinson disease' (MONDO:0017279) as a parent of 'Parkinson disease 13, autosomal dominant, susceptibility to' (MONDO:0012466)?

ValWood commented 1 week ago

Yes, based on the definition...