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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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NBIA3
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MONDO:0011638 |
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DBA15
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MONDO:0011639 |
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telomeric 22Q13 monosomy syndrome
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MONDO:0011652 |
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chromosome 22Q13.3 deletion syndrome
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MONDO:0011652 |
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deletion 22q13.3 syndrome
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MONDO:0011652 |
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CDG 1E
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MONDO:0012123 |
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DPM1-CDG
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MONDO:0012123 |
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carbohydrate-deficient glycoprotein syndrome type 1E
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MONDO:0012123 |
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congenital disorder of glycosylation, type Ie
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MONDO:0012123 |
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DPM1-CDG (CDG-Ie)
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MONDO:0012123 |
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CDG syndrome type Ie
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MONDO:0012123 |
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carbohydrate deficient glycoprotein syndrome type Ie
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MONDO:0012123 |
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DPM1 congenital disorder of glycosylation
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MONDO:0012123 |
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CDGIe
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MONDO:0012123 |
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SIDDT
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MONDO:0012124 |
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