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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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nystagmus 2, congenital, autosomal dominant
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MONDO:0008106 |
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Nystagmus congenital, motor 2
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MONDO:0008106 |
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oculodentodigital syndrome
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MONDO:0008111 |
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oculo-dento-digital syndrome
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MONDO:0008111 |
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odd syndrome
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MONDO:0008111 |
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ODDD syndrome
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MONDO:0008111 |
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oculodentoosseous dysplasia
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MONDO:0008111 |
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oculo-dento-digital dysplasia
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MONDO:0008111 |
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Oculo-Dento-Digital Dysplasia
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MONDO:0008111 |
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Schilbach-Rott syndrome
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MONDO:0008113 |
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hypotelorism cleft palate hypospadias
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MONDO:0008113 |
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blepharofacioskeletal syndrome
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MONDO:0008113 |
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cleft palate, hypotelorism, and hypospadias
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MONDO:0008113 |
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ocular hypotelorism, submucosal cleft palate, and hypospadias
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MONDO:0008113 |
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hypotelorism-cleft palate-hypospadias syndrome
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MONDO:0008113 |
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