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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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PLG-related hereditary angioedema with normal C1Inh
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Orphanet_537072 |
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Jejunal atresia-microcephaly-ocular anomalies syndrome
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Orphanet_506307 |
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Congenital vertebral-cardiac-renal anomalies syndrome
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Orphanet_521438 |
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Lens size anomaly of genetic origin
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Orphanet_522550 |
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Lens position anomaly of genetic origin
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Orphanet_522552 |
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Autosomal recessive anterior segment dysgenesis
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Orphanet_519388 |
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NMOSD with anti-AQP4 antibodies
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Orphanet_592850 |
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NMOSD with anti-MOG antibodies
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Orphanet_592856 |
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ADEM with anti-MOG antibodies
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Orphanet_592894 |
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Idiopathic infantile arterial calcification
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Orphanet_51608 |
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Idiopathic obliterative arteriopathy
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Orphanet_51608 |
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Occlusive infantile arteriopathy
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Orphanet_51608 |
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Cathepsin A-related arteriopathy-strokes-leukoencephalopathy
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Orphanet_575553 |
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Right coronary artery from left aortic sinus
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Orphanet_541454 |
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Left coronary artery from right aortic sinus
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Orphanet_541443 |
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