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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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Blue-dot cataract
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Orphanet_98989 |
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Cerulean cataract
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Orphanet_98989 |
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Coralliform cataract
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Orphanet_98990 |
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Huntington disease-like 2
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Orphanet_98934 |
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Distal-HMN type 6
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Orphanet_98920 |
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Corneal dystrophy Groenouw type I
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Orphanet_98962 |
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Corneal dystrophy Groenouw type II
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Orphanet_98969 |
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Primary familial amyloidosis of the cornea
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Orphanet_98957 |
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Acute motor and sensory axonal neuropathy
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Orphanet_98917 |
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Essential iris atrophy
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Orphanet_98981 |
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Spinal muscular atrophy with respiratory distress type 1
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Orphanet_98920 |
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Multiple system atrophy, parkinsonian type
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Orphanet_98933 |
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Acute motor-sensory axonal GBS
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Orphanet_98917 |
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Acute motor-sensory axonal Guillain-Barré syndrome
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Orphanet_98917 |
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Acute motor axonal neuropathy
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Orphanet_98918 |
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