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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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ARCA
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Orphanet_1172 |
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EOCA
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Orphanet_1177 |
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EOCARR
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Orphanet_1177 |
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SCAR2
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Orphanet_1170 |
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Behçet disease
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Orphanet_117 |
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CAPOS syndrome
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Orphanet_1171 |
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Gordon-Holmes syndrome
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Orphanet_1173 |
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Harding ataxia
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Orphanet_1177 |
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Ouvrier-Billson syndrome
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Orphanet_1179 |
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Early-onset cerebellar ataxia with retained tendon reflexes
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Orphanet_1177 |
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Autosomal recessive cerebellar ataxia
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Orphanet_1172 |
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X-linked progressive cerebellar ataxia
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Orphanet_1175 |
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Autosomal recessive cerebelloparenchymal disorder type 3
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Orphanet_1170 |
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Rare intestinal disease
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Orphanet_117569 |
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Cerebellar ataxia-ectodermal dysplasia syndrome
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Orphanet_1174 |
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