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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 familial neonatal-infantile seizures
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Orphanet_140927 |
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Primary central nervous system vasculitis
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Orphanet_140989 |
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Chronic infantile neurological cutaneous and articular syndrome
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Orphanet_1451 |
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Ectodermal dysplasia-acanthosis nigricans syndrome
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Orphanet_140936 |
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Congenital tubular nose
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Orphanet_141099 |
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Linear atrophoderma of Moulin
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Orphanet_140933 |
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Arteriovenous malformation of mandible
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Orphanet_141174 |
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Arteriovenous malformation of maxilla
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Orphanet_141171 |
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Isolated cleft of the ala nasi
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Orphanet_141242 |
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Spongy degeneration of the brain
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Orphanet_141 |
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Isolated angiitis of the central nervous system
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Orphanet_140989 |
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Primary angiitis of the central nervous system
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Orphanet_140989 |
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Primary vasculitis of the central nervous system
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Orphanet_140989 |
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Dermoid cyst of the face
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Orphanet_141051 |
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Dermoid cyst of the neck
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Orphanet_141046 |
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