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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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Non-syndromic accessory kydney
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Orphanet_652528 |
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Pregnancy and lactation-associated osteoporosis
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Orphanet_647823 |
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Non-syndromic unilateral lambdoid synostosis
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Orphanet_620113 |
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Non-syndromic bilateral lambdoid synostosis
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Orphanet_620178 |
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Autosomal dominant late-onset retinal degeneration
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Orphanet_67042 |
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Isolated anomalous left pulmonary artery
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Orphanet_658574 |
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Chronic lymphocytic leukemia
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Orphanet_67038 |
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Acute myeloid leukemia M7 in adult
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Orphanet_662934 |
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Acute megakaryoblastic leukemia in adult
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Orphanet_662934 |
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Acute megakaryocytic leukemia in adult
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Orphanet_662934 |
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Acute reversible leukoencephalopathy due to SLC13A3 deficiency
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Orphanet_615964 |
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Adult-onset progressive leukoencephalopathy-early-onset deafness
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Orphanet_652532 |
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Autosomal recessive limb-girdle muscular dystrophy type 2D
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Orphanet_62 |
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Autosomal recessive limb-girdle muscular dystrophy, type 28
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Orphanet_653725 |
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Lipomatous flat limited dorsal myeloschisis
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Orphanet_645300 |
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