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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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GSD type XI
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MONDO:0009216 |
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glycogen storage disease due to GLUT2 deficiency
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MONDO:0009216 |
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hepatorenal glycogenosis with renal Fanconi syndrome
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MONDO:0009216 |
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glycogenosis Fanconi EXACT
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MONDO:0009216 |
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glycogen storage disease XI
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MONDO:0009216 |
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glycogen storage disease 11
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MONDO:0009216 |
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glycogenosis, Fanconi type
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MONDO:0009216 |
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GLUT2 deficiency
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MONDO:0009216 |
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hepatic glycogenosis with amino aciduria and glucosuria
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MONDO:0009216 |
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glycogen storage disease type 11
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MONDO:0009216 |
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glycogen storage disease type XI
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MONDO:0009216 |
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hepatic glycogenosis with Fanconi nephropathy
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MONDO:0009216 |
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GSD type 11
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MONDO:0009216 |
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hepatorenal glycogenosis with renal fanconi syndrome
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MONDO:0009216 |
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GSD due to GLUT2 deficiency
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MONDO:0009216 |
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