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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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AIHA
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Orphanet_98375 |
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ETRS
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Orphanet_983 |
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FPLD
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Orphanet_98306 |
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Laminopathy
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Orphanet_98301 |
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Genetic lipodystrophy
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Orphanet_98305 |
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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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XY gonadal agenesis syndrome
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Orphanet_983 |
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Constitutional sideroblastic anemia
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Orphanet_98362 |
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Rare hemolytic anemia
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Orphanet_98363 |
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Autoimmune hemolytic anemia
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Orphanet_98375 |
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Constitutional hemolytic anemia due to acanthocytic disorder
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Orphanet_98366 |
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Constitutional hemolytic anemia due to acanthocytosis
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Orphanet_98366 |
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Hereditary stomatocytic disease
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Orphanet_98365 |
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Hemolytic anemia due to a disorder of glycolytic enzymes
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Orphanet_98372 |
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