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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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Aggressive primary cutaneous T-cell lymphoma
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Orphanet_178551 |
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Arginine vasopressin deficiency
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Orphanet_178029 |
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Primary cutaneous diffuse large B-cell lymphoma, leg type
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Orphanet_178544 |
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Moderate multiminicore disease with hand involvement
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Orphanet_178145 |
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Syndromic microphthalmia/anophthalmia due to OTX2 mutation
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Orphanet_178364 |
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Primary cutaneous epidermotropic cytotoxic CD8+ T-cell lymphoma
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Orphanet_178528 |
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Åland Islands eye disease
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Orphanet_178333 |
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Nablus mask-like facial syndrome
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Orphanet_178303 |
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Primary cutaneous follicle center lymphoma
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Orphanet_178540 |
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Mycosis fungoides-associated follicular mucinosis
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Orphanet_178512 |
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Congenital convex foot
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Orphanet_178382 |
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Congenital rocker-bottom foot
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Orphanet_178382 |
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Folliculotropic mycosis fungoides
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Orphanet_178512 |
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Primary cutaneous gamma/delta-positive T-cell lymphoma
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Orphanet_178533 |
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Hereditary prepubertal gynecomastia
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Orphanet_178345 |
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