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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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HIDS
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Orphanet_343 |
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MCOPS8
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Orphanet_3434 |
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Hyper-IgD syndrome
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Orphanet_343 |
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Microcephaly-brachydactyly-kyphoscoliosis syndrome
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Orphanet_3433 |
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Viljoen-Kallis-Voges syndrome
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Orphanet_3433 |
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MMEP syndrome
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Orphanet_3434 |
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Viljoen-Smart syndrome
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Orphanet_3434 |
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Uveomenigitic syndrome
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Orphanet_3437 |
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Vogt-Koyanagi-Harada disease
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Orphanet_3437 |
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Partial mevalonate kinase deficiency
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Orphanet_343 |
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Hyperimmunoglobulinemia D syndrome
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Orphanet_343 |
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DK phocomelia syndrome
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Orphanet_3439 |
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Von Voss-Cherstvoy syndrome
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Orphanet_3439 |
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Syndromic microphthalmia type 8
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Orphanet_3434 |
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Hyperimmunoglobulinemia D with periodic fever
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Orphanet_343 |
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