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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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2-methyl-3-hydroxybutyric aciduria, neonatal type
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Orphanet_391457 |
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HSD10 deficiency, neonatal type
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Orphanet_391457 |
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HSD10 disease, neonatal type
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Orphanet_391457 |
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MHBD deficiency, neonatal type
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Orphanet_391457 |
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MADD, severe neonatal type
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Orphanet_394529 |
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COASY protein-associated neurodegeneration
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Orphanet_397725 |
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Fatal post-viral neurodegenerative disorder
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Orphanet_391343 |
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Ovarian malignant non-epithelial tumor
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Orphanet_398940 |
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Intellectual disability-truncal obesity syndrome
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Orphanet_397941 |
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Bone necrosis of genetic origin
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Orphanet_399380 |
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Avascular necrosis of genetic origin
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Orphanet_399388 |
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Epithelial cancer of ovary
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Orphanet_398934 |
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Non-epithelial cancer of ovary
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Orphanet_398940 |
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Mucinous adenocarcinoma of ovary
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Orphanet_398961 |
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Immature teratoma of ovary
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Orphanet_398987 |
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