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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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DMDA1
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MONDO:0009677 |
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SCARMD
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MONDO:0009677 |
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SGCG autosomal recessive limb-girdle muscular dystrophy
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MONDO:0009677 |
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muscular dystrophy, limb-girdle, type 2C
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MONDO:0009677 |
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LGMD2C
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MONDO:0009677 |
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Maghrebian myopathy
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MONDO:0009677 |
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sarcoglycan, gamma, deficiency of
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MONDO:0009677 |
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limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
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MONDO:0009677 |
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muscular dystrophy, Duchenne-like
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MONDO:0009677 |
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Duchenne-like muscular dystrophy, autosomal recessive, type 1
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MONDO:0009677 |
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Adhalin deficiency, secondary
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MONDO:0009677 |
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autosomal recessive limb-girdle muscular dystrophy type 2C
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MONDO:0009677 |
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limb-girdle muscular dystrophy, type 2C
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MONDO:0009677 |
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Dmda
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MONDO:0009677 |
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deficiency of sarcoglycan gamma
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MONDO:0009677 |
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