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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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Teunissen-Cremers syndrome
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Orphanet_140917 |
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Lelis syndrome
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Orphanet_140936 |
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CLOVES syndrome
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Orphanet_140944 |
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Low-flow priapism
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Orphanet_140949 |
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STAR syndrome
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Orphanet_140952 |
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Conorenal syndrome
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Orphanet_140969 |
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Saldino-Mainzer syndrome
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Orphanet_140969 |
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RHYNS syndrome
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Orphanet_140976 |
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Oral-facial-digital syndrome
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Orphanet_140997 |
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Orofaciodigital syndrome
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Orphanet_140997 |
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LGMD type 2J
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Orphanet_140922 |
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Brachydactyly type B2
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Orphanet_140908 |
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Palmoplantar hyperkeratosis, Nagashima type
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Orphanet_140966 |
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Palmoplantar keratoderma, Nagashima type
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Orphanet_140966 |
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Titin-related LGMD R10
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Orphanet_140922 |
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