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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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Interstitial granulomatous dermatitis with arthritis
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Orphanet_79099 |
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Acquired lipoatrophic diabetes
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Orphanet_79086 |
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PNPO-related neonatal epileptic encephalopathy
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Orphanet_79096 |
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Acquired generalized lipodystrophy
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Orphanet_79086 |
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Acquired partial lipodystrophy
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Orphanet_79087 |
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Progressive cephalothoracic lipodystrophy
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Orphanet_79087 |
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Familial partial lipodystrophy type 1
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Orphanet_79084 |
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Familial partial lipodystrophy type 3
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Orphanet_79083 |
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Familial partial lipodystrophy, Köbberling type
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Orphanet_79084 |
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Subacute necrotizing myelitis
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Orphanet_79093 |
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Subacute angiohypertrophic myelomalacia
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Orphanet_79093 |
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Angiodysgenetic necrotizing myelopathy
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Orphanet_79093 |
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Inclusion body myopathy type 3
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Orphanet_79091 |
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Subacute ascending necrotizing myelitis
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Orphanet_79093 |
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Juvenile polyposis of infancy
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Orphanet_79076 |
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