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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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ARCL3A
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MONDO:0009053 |
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ALDH18A1-related de Barsy syndrome
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MONDO:0009053 |
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progeroid syndrome of De Barsy
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MONDO:0009053 |
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cutis laxa, autosomal recessive, type 3A
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MONDO:0009053 |
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autosomal recessive cutis laxa type IIIA
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MONDO:0009053 |
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De Barsy syndrome a
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MONDO:0009053 |
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cutis laxa, corneal clouding, and intellectual disability
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MONDO:0009053 |
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cutis laxa, autosomal recessive, type IIIA
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MONDO:0009053 |
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cutis laxa, corneal clouding, and mental retardation
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MONDO:0009053 |
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P5CS deficiency
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MONDO:0009053 |
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Delta-1-pyrroline 5-carboxylate synthetase deficiency
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MONDO:0009053 |
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neurocutaneous syndrome, Bicknell type
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MONDO:0009053 |
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De Barsy syndrome A
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MONDO:0009053 |
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