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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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Dermatoleukodystrophy
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Orphanet_1659 |
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EIHI
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Orphanet_165991 |
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Cutis laxa-leukodystrophy
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Orphanet_1659 |
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Traumatic myiasis
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Orphanet_165955 |
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Wound myiasis
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Orphanet_165955 |
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Cavitary myiasis
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Orphanet_165958 |
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Exercise-induced hyperinsulinism
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Orphanet_165991 |
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Hyperinsulinemic hypoglycemia, diazoxide-resistant diffuse form
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Orphanet_165988 |
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Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form
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Orphanet_165985 |
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Diazoxide-sensitive diffuse hyperinsulinism
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Orphanet_165985 |
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Diazoxide-resistant diffuse hyperinsulinism
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Orphanet_165988 |
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Exercise-induced hyperinsulinemic hypoglycemia
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Orphanet_165991 |
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Hyperinsulinism due to SLC16A1 deficiency
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Orphanet_165991 |
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Hyperinsulinism due to monocarboxylate transporter 1 deficiency
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Orphanet_165991 |
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