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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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Acquired lipodystrophy
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Orphanet_98307 |
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Hereditary stomatocytosis
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Orphanet_98365 |
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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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Pontoneocerebellar atrophy
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Orphanet_98523 |
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Pontoneocerebellar hypoplasia
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Orphanet_98523 |
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Anophthalmia-microphthalmia syndrome
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Orphanet_98555 |
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Syndromic aniridia
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Orphanet_98557 |
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Microblepharon-ablephara syndrome
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Orphanet_98563 |
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Syndromic ankyloblepharon
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Orphanet_98565 |
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Congenital ectropion
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Orphanet_98570 |
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Secondary ectropion
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Orphanet_98571 |
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