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created at |
2021-12-13 15:49:09 UTC |
updated at |
2021-12-13 16:09:58 UTC |
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Mondo Disease Ontology (Mondo).
Mondo aims to harmonizes disease definitions across the world. For more details on this ontology see:
Mondo website: https://monarch-initiative.github.io/mondo
OBO Foundry Mondo page: http://obofoundry.org/ontology/mondo.html
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24,745 entries
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There is 0 pattern entry.
MEDNIK syndrome
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0012251 |
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MEGF10-Related Myopathy
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0013731 |
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MEGF8-related Carpenter syndrome
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0013998 |
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MEHMO syndrome
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0010258 |
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MELAS syndrome
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0010789 |
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MEND syndrome
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0010498 |
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MERRF syndrome
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0010790 |
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MGAT2-CDG
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0008908 |
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MHC class I deficiency
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0011476 |
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MHC class II deficiency
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0008855 |
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MIRAGE syndrome
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0014888 |
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MIT family translocation renal cell carcinoma
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0017886 |
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MME-related autosomal dominant Charcot Marie Tooth disease type 2
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0044657 |
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MMEP syndrome
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0011045 |
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MOGS-CDG
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0011629 |
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