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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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CMD1A
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Orphanet_258 |
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MDC1A
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Orphanet_258 |
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Mycetoma
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Orphanet_2583 |
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Madura foot
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Orphanet_2583 |
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Ataxia-pancytopenia syndrome
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Orphanet_2585 |
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Myelocerebellar disorder
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Orphanet_2585 |
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MPO deficiency
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Orphanet_2587 |
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Myeloperoxidase deficiency
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Orphanet_2587 |
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Myhre syndrome
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Orphanet_2588 |
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Mycosis fungoides, Alibert-Bazin type
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Orphanet_2584 |
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Laminin subunit alpha 2-related congenital muscular dystrophy
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Orphanet_258 |
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Myalgia-eosinophilia syndrome associated with tryptophan
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Orphanet_2582 |
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Congenital muscular dystrophy due to laminin alpha2 deficiency
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Orphanet_258 |
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Congenital muscular dystrophy type 1A
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Orphanet_258 |
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Classic mycosis fungoides
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Orphanet_2584 |
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