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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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CMT2P
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Orphanet_300319 |
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Dup(11)p(15.4)
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Orphanet_300305 |
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FACU
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Orphanet_300359 |
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PLAID
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Orphanet_300359 |
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PPBL
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Orphanet_300324 |
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Pyknoachondrogenesis
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Orphanet_3003 |
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X-LAG
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Orphanet_300373 |
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Camera syndrome
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Orphanet_3003 |
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Trisomy 11p15.4
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Orphanet_300305 |
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Huppke-Brendel syndrome
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Orphanet_300313 |
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Autosomal SLE
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Orphanet_300345 |
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Familial SLE
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Orphanet_300345 |
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X-linked acrogigantism
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Orphanet_300373 |
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Pituitary carcinoma
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Orphanet_300385 |
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Persistent polyclonal B-cell lymphocytosis
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Orphanet_300324 |
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