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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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PMED
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Orphanet_352596 |
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SCAR14
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Orphanet_352403 |
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SPARCA
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Orphanet_352403 |
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SPARCA1
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Orphanet_352403 |
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Scleredema
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Orphanet_352763 |
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MEGDEL syndrome
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Orphanet_352328 |
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PEO-myopathy-emaciation syndrome
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Orphanet_352447 |
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AUTS2 syndrome
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Orphanet_352490 |
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Oncogenic osteomalacia
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Orphanet_352540 |
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Tumor-induced osteomalacia
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Orphanet_352540 |
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Bainbridge-Ropers syndrome
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Orphanet_352577 |
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Monosomy 16q24.1
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Orphanet_352629 |
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Phalangeal osteolysis
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Orphanet_352636 |
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CLN13 disease
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Orphanet_352709 |
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FILS syndrome
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Orphanet_352712 |
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