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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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MTO-deficiency
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Orphanet_562538 |
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McCune-Albright syndrome
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Orphanet_562 |
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HO-1 deficiency
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Orphanet_562509 |
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CLIFAHDD syndrome
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Orphanet_562528 |
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MRAMS syndrome
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Orphanet_562559 |
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PBC/PSC and AIH overlap syndrome
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Orphanet_562639 |
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Heme oxygenase-1 deficiency
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Orphanet_562509 |
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Methanethiol oxidase deficiency
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Orphanet_562538 |
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Autosomal recessive extra-oral halitosis
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Orphanet_562538 |
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Overlap syndromes of autoimmune liver diseases
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Orphanet_562639 |
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Gonadotropin-independent female-limited sexual precocity
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Orphanet_562 |
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