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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.
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GNE myopathy
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0011603 |
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GOMBO syndrome
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0009298 |
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GRFoma
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0019955 |
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GRID2-related autosomal dominant spinocerebellar ataxia
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0000563 |
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GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
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0035122 |
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GTP cyclohydrolase I deficiency
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0100184 |
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GTP cyclohydrolase I deficiency with hyperphenylalaninemia
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0100186 |
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GUCY2D retinopathy
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0100454 |
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Gabriele de Vries syndrome
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0044738 |
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Gaisbock syndrome
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0019538 |
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Galloway-Mowat syndrome
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0009627 |
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Galloway-Mowat syndrome 1
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0033005 |
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Galloway-Mowat syndrome 2, X-linked
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0033006 |
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Galloway-Mowat syndrome 3
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0033007 |
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Galloway-Mowat syndrome 4
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0033008 |
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