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| created at |
2019-07-11 18:15:35 UTC |
| updated at |
2025-12-23 18:38:35 UTC |
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Diseases and disorders as defined in the MONDO ontology, the version 2025-01-07.
Only the terms under the node "disease" (MONDO_0000001) are included.
All identifiers use the CURIE format with the MONDO: prefix (e.g., MONDO:12345),
which corresponds to the full IRI namespace http://purl.obolibrary.org/obo/MONDO_.
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112,359 entries
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There is 0 pattern entry.
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neuropathy, hereditary sensory and autonomic, type 2B
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MONDO:0013142 |
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CANDF4
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MONDO:0013140 |
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HSAN2B
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MONDO:0013142 |
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Oropouche virus caused disease or disorder
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MONDO:0000345 |
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Oropouche virus infectious disease
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MONDO:0000345 |
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Balkan hemorrhagic fever
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MONDO:0000346 |
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disorder of methionine catabolism
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MONDO:0000351 |
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hypermethioninemia
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MONDO:0000351 |
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rare inborn error of methionine catabolic process
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MONDO:0000351 |
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inborn methionine catabolic process disorder
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MONDO:0000351 |
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inborn error of methionine catabolic process
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MONDO:0000351 |
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Ullrich congenital muscular dystrophy
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MONDO:0000355 |
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Ullrich disease
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MONDO:0000355 |
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late onset scleroatonic familial myopathy (subtype)
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MONDO:0000355 |
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congenital muscular dystrophy, Ullrich type
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MONDO:0000355 |
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