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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 progressive cerebellar ataxia
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0010547 |
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X-linked pure spastic paraplegia
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0017912 |
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X-linked recessive disease
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0020605 |
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X-linked recessive mitochondrial myopathy
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0100138 |
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X-linked recessive ocular albinism
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0021019 |
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X-linked reticulate pigmentary disorder
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0010523 |
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X-linked retinal dysplasia
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0010722 |
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X-linked retinoschisis
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0010725 |
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X-linked scapuloperoneal muscular dystrophy
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0010400 |
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X-linked severe congenital neutropenia
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0010294 |
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X-linked sideroblastic anemia 1
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0020721 |
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X-linked sideroblastic anemia with ataxia
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0010524 |
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X-linked spasticity-intellectual disability-epilepsy syndrome
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0017856 |
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X-linked spermatogenic failure 1
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0056795 |
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X-linked spinocerebellar ataxia type 3
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0010529 |
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