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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.
DGI-2
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Orphanet_166260 |
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DI-2
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Orphanet_166260 |
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Dirofilariasis
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Orphanet_166291 |
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ODCD
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Orphanet_166272 |
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Odontochondrodysplasia
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Orphanet_166272 |
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Restrictive dermopathy
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Orphanet_1662 |
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Capdepont teeth
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Orphanet_166260 |
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Goldblatt chondrodysplasia
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Orphanet_166272 |
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Goldblatt syndrome
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Orphanet_166272 |
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Suarez-Stickler syndrome
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Orphanet_166277 |
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Dentinogenesis imperfecta, Shields type 2
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Orphanet_166260 |
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Dentinogenesis imperfecta, Shields type 3
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Orphanet_166265 |
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Lethal restrictive dermopathy
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Orphanet_1662 |
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Benign partial epilepsy of infancy with complex partial seizures
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Orphanet_166299 |
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Benign non-familial infantile seizures
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Orphanet_166295 |
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