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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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BRIC
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Orphanet_65682 |
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ETMR
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Orphanet_656417 |
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JMADUE
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Orphanet_65684 |
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Genetic SRNS
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Orphanet_656 |
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Atrophic papulosis
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Orphanet_656071 |
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Degos disease
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Orphanet_656071 |
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Köhlmeier-Degos disease
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Orphanet_656071 |
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Vaginal atresia
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Orphanet_65681 |
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Summerskill-Walshe-Tygstrup syndrome
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Orphanet_65682 |
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Hirayama disease
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Orphanet_65684 |
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Monomelic amyotrophy
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Orphanet_65684 |
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PBX1-related syndromic CAKUT
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Orphanet_656130 |
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Benign focal amyotrophy
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Orphanet_65684 |
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Juvenile muscular atrophy of distal upper extremity
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Orphanet_65684 |
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Juvenile muscular atrophy of the distal upper limb
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Orphanet_65684 |
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