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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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Stoll-Alembik-Finck syndrome
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Orphanet_3200 |
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Stoll-Kieny-Dott syndrome
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Orphanet_3201 |
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Hereditary xerocytosis
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Orphanet_3202 |
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Maternally-inherited SPG
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Orphanet_320360 |
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Stormorken syndrome
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Orphanet_3204 |
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Stormorken-Sjaastad-Langslet syndrome
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Orphanet_3204 |
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Thrombocytopathy-asplenia-miosis syndrome
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Orphanet_3204 |
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Encephalofacial angiomatosis
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Orphanet_3205 |
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Encephalotrigeminal angiomatosis
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Orphanet_3205 |
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Sturge-Weber syndrome
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Orphanet_3205 |
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Sturge-Weber-Dimitri syndrome
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Orphanet_3205 |
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Sturge-Weber-Krabbe angiomatosis
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Orphanet_3205 |
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Sturge-Weber-Krabbe syndrome
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Orphanet_3205 |
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Stüve-Wiedemann dysplasia
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Orphanet_3206 |
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Stüve-Wiedemann syndrome
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Orphanet_3206 |
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