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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 inactivation, familial skewed, 2
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0026426 |
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X small rings
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0019926 |
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X-linked Alport syndrome
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0010520 |
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X-linked Ehlers-Danlos syndrome
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0010586 |
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X-linked Emery-Dreifuss muscular dystrophy
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0010680 |
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X-linked Opitz G/BBB syndrome
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0010222 |
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X-linked acrogigantism due to Xq26 microduplication
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0010491 |
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X-linked acrogigantism due to a point mutation
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0018665 |
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X-linked adrenal hypoplasia congenita
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0010264 |
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X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
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0010522 |
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X-linked calvarial hyperostosis
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0010541 |
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X-linked central congenital hypothyroidism with late-onset testicular enlargement
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0010475 |
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X-linked centronuclear myopathy
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0010683 |
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X-linked cerebellar ataxia
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0016612 |
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X-linked cerebral adrenoleukodystrophy
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0010247 |
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