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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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Sex-chromosome number anomaly
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Orphanet_98156 |
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Allosome structural anomaly
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Orphanet_98157 |
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Sex-chromosome structural anomaly
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Orphanet_98157 |
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Eyelid border anomaly
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Orphanet_98564 |
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Rare eyebrow/eyelashes anomaly
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Orphanet_98594 |
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Rare refraction anomaly
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Orphanet_98618 |
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Lens size anomaly
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Orphanet_98652 |
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Lens position anomaly
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Orphanet_98653 |
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Lens shape anomaly
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Orphanet_98655 |
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Heart position anomaly
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Orphanet_98716 |
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Atrioventricular valve anomaly
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Orphanet_98720 |
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Ascending aorta anomaly
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Orphanet_98725 |
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Congenital aorta, aortic arch or pulmonary arteries anomaly
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Orphanet_98724 |
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Acquired epileptic aphasia
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Orphanet_98818 |
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Unilateral pulmonary artery agenesis
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Orphanet_980 |
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