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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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Hereditary motor and sensory neuropathy, Lom type
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Orphanet_99950 |
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Hereditary motor and sensory neuropathy, Russe Type
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Orphanet_99953 |
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Interventricular septum aneurysm
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Orphanet_99092 |
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Atrial septal aneurysm
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Orphanet_99107 |
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Encircling double aortic arch
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Orphanet_99075 |
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Persistent fifth aortic arch
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Orphanet_99076 |
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VSD with aortic insufficiency
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Orphanet_99094 |
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Cervical aortic arch
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Orphanet_99079 |
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Right aortic arch
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Orphanet_99081 |
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Congenital coronary arterial orifice stenosis or atresia
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Orphanet_99087 |
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Branch pulmonary artery stenosis
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Orphanet_99084 |
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Coronary sinus atresia
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Orphanet_99118 |
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Lymphedema-posterior choanal atresia syndrome
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Orphanet_99141 |
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Left ventricular-to-right atrial communication
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Orphanet_99095 |
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Unbalanced complete atrioventricular canal
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Orphanet_99067 |
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