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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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congenital disorder of glycosylation type 2g
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MONDO:0012637 |
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CDG2G
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MONDO:0012637 |
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CDG syndrome type IIg
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MONDO:0012637 |
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congenital disorder of glycosylation type IIg
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MONDO:0012637 |
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microphthalmia-brain atrophy syndrome
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MONDO:0012638 |
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microphthalmia syndromic 10
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MONDO:0012638 |
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microphthalmia, syndromic 10
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MONDO:0012638 |
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microphthalmia and brain atrophy
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MONDO:0012638 |
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MOBA syndrome
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MONDO:0012638 |
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MCOPS10
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MONDO:0012638 |
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syndromic microphthalmia type 10
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MONDO:0012638 |
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IBD15
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MONDO:0012837 |
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CDG-Iq
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MONDO:0012885 |
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congenital disorder of glycosylation type Iq
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MONDO:0012885 |
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inflammatory bowel disease 22
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MONDO:0012886 |
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