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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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IgA pemphigus
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Orphanet_555905 |
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Hypotrichosis simplex
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Orphanet_55654 |
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Pneumococcal meningitis
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Orphanet_55655 |
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Non-syndromic ARM
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Orphanet_557 |
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Oculo-skeleto-dental syndrome
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Orphanet_557003 |
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Oculoskeletodental syndrome
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Orphanet_557003 |
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Marfan syndrome
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Orphanet_558 |
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Idiopathic gastroparesis
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Orphanet_558411 |
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Marinesco-Sjögren syndrome
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Orphanet_559 |
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Hereditary ochronosis
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Orphanet_56 |
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Marshall syndrome
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Orphanet_560 |
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Marshall-Smith syndrome
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Orphanet_561 |
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FOXG1 syndrome
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Orphanet_561854 |
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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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