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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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X-linked complicated corpus callosum dysgenesis
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Orphanet_1497 |
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Cervical dermoid cyst
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Orphanet_141046 |
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Facial dermoid cyst
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Orphanet_141051 |
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Nasolacrimal duct cyst
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Orphanet_141083 |
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Nasal dermoid cyst
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Orphanet_141103 |
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Congenital laryngeal cyst
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Orphanet_141124 |
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Digestive duplication cyst of the tongue
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Orphanet_141071 |
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Enteric duplication cyst of the tongue
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Orphanet_141071 |
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Foregut duplication cyst of the tongue
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Orphanet_141071 |
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Gastric duplication cyst of the tongue
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Orphanet_141071 |
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Autosomal dominant dHMN
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Orphanet_140465 |
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Autosomal recessive dHMN
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Orphanet_140468 |
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Autosomal recessive dSMA
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Orphanet_140468 |
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Corneal dystrophy-perceptive deafness syndrome
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Orphanet_1490 |
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Atrial septal defect
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Orphanet_1478 |
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