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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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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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Familial hyperinflammatory lymphoproliferative immunodeficiency
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Orphanet_619953 |
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Inherited cancer-predisposing lymphoproliferative syndrome
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Orphanet_664450 |
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CPP in male
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Orphanet_649929 |
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Non-syndromic cloacal malformation
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Orphanet_600998 |
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Open split-cord malformation
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Orphanet_645388 |
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Congenital limb malformation
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Orphanet_68378 |
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Split cord malformation associated with myeloschisis
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Orphanet_645393 |
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Split cord malformation type 1.5
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Orphanet_633076 |
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Non-syndromic anorectal malformation with H-type fistula
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Orphanet_601033 |
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Non-syndromic anorectal malformation with anal stenosis
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Orphanet_601008 |
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Non-syndromic anorectal malformation with bladder neck fistula
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Orphanet_600984 |
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Non-syndromic anorectal malformation with cutaneous fistula
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Orphanet_600952 |
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Non-syndromic anorectal malformation with no fistula
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Orphanet_601002 |
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