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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.
RHYNS syndrome
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Orphanet_140976 |
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Oral-facial-digital syndrome
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Orphanet_140997 |
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Orofaciodigital syndrome
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Orphanet_140997 |
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ACY2 deficiency
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Orphanet_141 |
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Aspartoacylase deficiency
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Orphanet_141 |
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Canavan disease
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Orphanet_141 |
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Cervicofacial fibrochondroma
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Orphanet_141067 |
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Oropharyngeal teratoma
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Orphanet_141077 |
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Nasolacrimal mucocele
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Orphanet_141083 |
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Double nose
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Orphanet_141091 |
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Accessory nostril
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Orphanet_141096 |
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Supernumerary nostril
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Orphanet_141096 |
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Proboscis lateralis
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Orphanet_141099 |
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Nasopharyngeal teratoma
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Orphanet_141107 |
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Nasal glioma
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Orphanet_141112 |
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