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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 AHC
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Orphanet_95702 |
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Thyroid ectopia
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Orphanet_95712 |
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Thyroid dyshormonogenesis
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Orphanet_95716 |
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Thyroid hemiagenesis
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Orphanet_95719 |
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Thyroid hypoplasia
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Orphanet_95720 |
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Acro-renal-mandibular syndrome
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Orphanet_958 |
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Isolated levocardia
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Orphanet_95854 |
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Acro-renal-ocular syndrome
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Orphanet_959 |
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Acrofacial dysostosis, Weyers type
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Orphanet_952 |
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X-linked congenital adrenal hypoplasia
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Orphanet_95702 |
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Tricuspid valve agenesis
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Orphanet_95457 |
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Congenital major airway collapse
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Orphanet_95430 |
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Congenital coronary aneurysm
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Orphanet_95491 |
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Arterial duct anomaly
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Orphanet_95485 |
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Atrial appendage anomaly
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Orphanet_95510 |
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