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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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Polycythemia
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Orphanet_98427 |
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Pulmonary agenesis
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Orphanet_984 |
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Secondary erythrocytosis
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Orphanet_98428 |
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Secondary polycythemia
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Orphanet_98428 |
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Muscular dystrophy
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Orphanet_98473 |
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Metabolic myopathy
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Orphanet_98486 |
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Hereditary combined deficiency of factors II, VII, IX and X
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Orphanet_98434 |
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Alpha granule disease
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Orphanet_98455 |
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Delta granule disease
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Orphanet_98456 |
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Dense granule disease
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Orphanet_98456 |
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Skeletal muscle disease
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Orphanet_98472 |
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Neuromuscular junction disease
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Orphanet_98491 |
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Rare coagulation disorder
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Orphanet_98429 |
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Acquired neuromuscular junction disease
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Orphanet_98494 |
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Genetic neuromuscular junction disease
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Orphanet_98495 |
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