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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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SPG18
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MONDO:0012639 |
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hereditary spastic paraplegia 18
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MONDO:0012639 |
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spastic paraplegia 18
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MONDO:0012639 |
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spastic paraplegia 18, autosomal recessive
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MONDO:0012639 |
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autosomal recessive spastic paraplegia 18
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MONDO:0012639 |
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autosomal recessive spastic paraplegia type 18
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MONDO:0012639 |
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ERLIN2 autosomal recessive complex spastic paraplegia
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MONDO:0012639 |
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hereditary spastic paraplegia type 18
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MONDO:0012639 |
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