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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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Benign recurrent intrahepatic cholestasis
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Orphanet_65682 |
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Non-syndromic supernumerary kidney
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Orphanet_652528 |
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Non-syndromic accessory kidneys
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Orphanet_652528 |
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Non-syndromic supernumerary kidneys
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Orphanet_652528 |
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Non-syndromic accessory kydney
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Orphanet_652528 |
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Isolated anomalous left pulmonary artery
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Orphanet_658574 |
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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 28
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Orphanet_653725 |
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Sclerosing lymphocytic lobulitis
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Orphanet_653698 |
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Enteropathy-associated T-cell lymphoma type 2
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Orphanet_652658 |
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Nodal T-cell lymphoma with TFH phenotype
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Orphanet_652650 |
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Nodal TFH lymphoma, follicular type
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Orphanet_652650 |
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Autosomal dominant multiple pterygium syndrome
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Orphanet_65743 |
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Multiple endocrine neoplasia type 1
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Orphanet_652 |
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Multiple endocrine neoplasia type 2
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Orphanet_653 |
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