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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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X-linked congenital hemolytic anemia
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0060455 |
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X-linked congenital stationary night blindness
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0044749 |
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X-linked corneal dermoid
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0010579 |
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X-linked deafness
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0020768 |
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X-linked diffuse leiomyomatosis-Alport syndrome
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0010641 |
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X-linked disease
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0000425 |
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X-linked distal hereditary motor neuropathy
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0018451 |
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X-linked distal spinal muscular atrophy type 3
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0010338 |
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X-linked dominant chondrodysplasia, Chassaing-Lacombe type
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0010463 |
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X-linked dominant disease
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0020604 |
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X-linked dominant hypophosphatemic rickets
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0010619 |
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X-linked dominant intellectual disability-epilepsy syndrome
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0019770 |
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X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
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0010444 |
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X-linked dystonia-parkinsonism
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0010747 |
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X-linked endothelial corneal dystrophy
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0010426 |
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