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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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Hereditary chronic pancreatitis
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Orphanet_676 |
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Recurrent respiratory papillomatosis
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Orphanet_60032 |
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Pruritic urticarial papules and plaques of pregnancy
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Orphanet_64745 |
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Benign atrophic papulosis
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Orphanet_656085 |
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Malignant atrophic papulosis
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Orphanet_679 |
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Hypokalemic periodic paralysis
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Orphanet_681 |
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Hyperkalemic periodic paralysis
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Orphanet_682 |
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Hereditary spastic paraparesis
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Orphanet_685 |
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Familial spastic paraplegia
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Orphanet_685 |
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Hereditary spastic paraplegia
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Orphanet_685 |
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Focal intestinal perforation
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Orphanet_645793 |
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Spontaneous intestinal perforation
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Orphanet_645793 |
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Twin-reversed arterial perfusion sequence
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Orphanet_617297 |
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Familial hyperkalemic periodic paralysis
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Orphanet_682 |
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Primary hyperkalemic periodic paralysis
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Orphanet_682 |
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