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| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
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X-linked myopathy with excessive autophagy
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Orphanet_25980 |
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Pseudopapillary neurocytoma with glial differentiation
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Orphanet_251962 |
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Exercise intolerance with lactic acidosis
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Orphanet_254843 |
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OXPHOS disease with no known mechanism
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Orphanet_254822 |
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Oculoauriculovertebral spectrum with radial defects
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Orphanet_2549 |
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Mitochondrial myopathy with reversible COX deficiency
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Orphanet_254864 |
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Mitochondrial myopathy with reversible complex IV deficiency
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Orphanet_254864 |
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Genetic hyperferritinemia without iron overload
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Orphanet_254704 |
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