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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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Chronic relapsing inflammatory optic neuritis
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Orphanet_499085 |
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Aquagenic palmoplantar keratoderma
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Orphanet_498359 |
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Non-syndromic longitudinal limb defect
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Orphanet_498457 |
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Rare hyperkinetic movement disorder
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Orphanet_494457 |
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Keratoderma hereditarium mutilans
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Orphanet_494 |
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Isolated optic neuritis
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Orphanet_499096 |
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Autoimmune/inflammatory optic neuropathy
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Orphanet_499047 |
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Ocular anomalies-axonal neuropathy-developmental delay syndrome
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Orphanet_496790 |
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Recurrent idiopathic neuroretinitis
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Orphanet_499103 |
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Epidermolytic epidermal nevus
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Orphanet_497737 |
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Mutilating keratoderma of Vohwinkel
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Orphanet_494 |
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Phyllodes type of atypical prostatic hyperplasia
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Orphanet_498228 |
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Mother-to-child transmission of syphilis
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Orphanet_499009 |
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Aquagenic wrinkling of the palms
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Orphanet_498359 |
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Cystosarcoma phyllodes of the prostate
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Orphanet_498228 |
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