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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.
Complete AVSD-tetralogy of Fallot
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Orphanet_99068 |
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Abnormal number of coronary ostia
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Orphanet_99089 |
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Abnormal origin of right or left pulmonary artery from the aorta
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Orphanet_99050 |
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Reticular dystrophy of the retinal pigment epithelium
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Orphanet_99002 |
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Congenital anomaly of the tricuspid valve chordae
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Orphanet_99055 |
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Congenital anomaly of tricuspid chordae tendineae
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Orphanet_99055 |
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Congenital anomaly of tricuspid tendinous chords
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Orphanet_99055 |
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Straddling and/or overriding mitral valve
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Orphanet_99064 |
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Congenital stenosis or atresia of a coronary ostium
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Orphanet_99087 |
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X-linked spastic paraplegia type 2
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Orphanet_99015 |
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Cor triatriatum sinister
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Orphanet_99099 |
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Double outlet right ventricle, Fallot type
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Orphanet_99043 |
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Complete atrioventricular septal defect-tetralogy of Fallot
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Orphanet_99068 |
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Cor triatriatum sinistrum
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Orphanet_99099 |
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Tunnel subaortic stenosis
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Orphanet_99053 |
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