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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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FPLCA
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Orphanet_353220 |
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Gamma-sarcoglycanopathy
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Orphanet_353 |
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LGMD2C
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Orphanet_353 |
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Orodynia
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Orphanet_353253 |
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Stomatodynia
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Orphanet_353253 |
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Stomatopyrosis
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Orphanet_353253 |
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VPTR
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Orphanet_353356 |
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AGC1 deficiency
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Orphanet_353217 |
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Oral dysesthesia
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Orphanet_353253 |
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Roifman syndrome
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Orphanet_353298 |
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Aneurysmal telangiectasia
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Orphanet_353344 |
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LGMD type 2C
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Orphanet_353 |
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Gamma-sarcoglycan-related LGMD R5
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Orphanet_353 |
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Congenital arteriovenous anastomoses of the retina
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Orphanet_353334 |
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Congenital retinal arteriovenous anastomoses
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Orphanet_353334 |
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