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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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Glycogenosis type IXd
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Orphanet_715 |
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GSD type IXe
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Orphanet_715 |
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Glycogenosis type IXe
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Orphanet_715 |
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Glycogen storage disease type 9D
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Orphanet_715 |
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Glycogen storage disease type 9E
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Orphanet_715 |
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Glycogen storage disease type IXd
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Orphanet_715 |
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Glycogen storage disease type IXe
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Orphanet_715 |
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Psychogenic movement disorders
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Orphanet_71519 |
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Obesity due to melanocortin 4 receptor deficiency
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Orphanet_71529 |
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GSD due to muscle phosphorylase kinase deficiency
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Orphanet_715 |
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Glycogenosis due to muscle phosphorylase kinase deficiency
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Orphanet_715 |
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Obesity due to pro-opiomelanocortin deficiency
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Orphanet_71526 |
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Obesity due to prohormone convertase I deficiency
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Orphanet_71528 |
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Benign paroxysmal torticollis of infancy
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Orphanet_71518 |
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