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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.
Rare tumor of neuroepithelial tissue
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Orphanet_251558 |
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Embryonal tumor of neuroepithelial tissue
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Orphanet_251852 |
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Pineal tumor of neuroepithelial tissue
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Orphanet_251905 |
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Glial tumor of neuroepithelial tissue with unknown origin
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Orphanet_251668 |
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Primary melanoma of the CNS
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Orphanet_252050 |
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Primary melanoma of the central nervous system
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Orphanet_252050 |
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Papillary tumor of the pineal region
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Orphanet_251915 |
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Persistent fever/inflammation of unknown origin
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Orphanet_251332 |
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Autosomal dominant optic atrophy and peripheral neuropathy
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Orphanet_250932 |
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Polymicrogyria with optic nerve hypoplasia
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Orphanet_250972 |
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Lichen planus pemphigoides
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Orphanet_254478 |
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Idiopathic recurrent pericarditis
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Orphanet_251307 |
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Idiopathic relapsing pericarditis
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Orphanet_251307 |
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Isolated oxidative phosphorylation complex disorder
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Orphanet_254846 |
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Combined oxidative phosphorylation defect type 2
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Orphanet_254920 |
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