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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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Neuroferritinopathy; basal ganglia disease, adult-onset
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MONDO:0011638 |
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hereditary ferritinopathy
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MONDO:0011638 |
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NBIA3
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MONDO:0011638 |
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neuroferritinopathy
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MONDO:0011638 |
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basal ganglia disease, adult-onset
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MONDO:0011638 |
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basal ganglia disease adult-onset
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MONDO:0011638 |
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neurodegeneration with brain iron accumulation 3
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MONDO:0011638 |
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ferritin-related neurodegeneration
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MONDO:0011638 |
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neurodegeneration with brain iron accumulation type 3
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MONDO:0011638 |
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adult basal ganglia disease
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MONDO:0011638 |
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