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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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PR interval, variation 1N
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0007175 |
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Pearson syndrome
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0010797 |
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PRKAR1B-related neurodegenerative dementia with intermediate filaments
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0018475 |
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PRPS1 deficiency disorder
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0100061 |
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PSAT deficiency
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0012596 |
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PSPH deficiency
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0013531 |
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PTEN hamartoma tumor syndrome
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0017623 |
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PUM1-associated developmental disability-ataxia-seizure syndrome
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0035117 |
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PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
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0018580 |
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PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation
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0014512 |
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PYCR1-related de Barsy syndrome
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0013755 |
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PYCR2-related microcephaly-progressive leukoencephalopathy
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0018825 |
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Pacinian tumor
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0002383 |
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Paganini-Miozzo syndrome
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0026724 |
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Paget disease
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0021165 |
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