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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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Desquamative interstitial pneumonia
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Orphanet_98852 |
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Bilateral perisylvian polymicrogyria
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Orphanet_98889 |
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Transient acquired pure red cell aplasia
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Orphanet_98871 |
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Primary acquired pure red cell aplasia
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Orphanet_98872 |
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X-linked complex spastic paraplegia
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Orphanet_98888 |
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X-linked complicated spastic paraplegia
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Orphanet_98888 |
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Werner mesomelic spectrum
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Orphanet_988 |
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Absent tibia-polydactyly syndrome
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Orphanet_988 |
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Unclassified myelodysplastic syndrome
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Orphanet_98827 |
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Angioendotheliomatosis proliferans systemisata
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Orphanet_98839 |
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Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
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Orphanet_988 |
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Optic atrophy type 2
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Orphanet_98890 |
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Charcot-Marie-Tooth disease type 2B1
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Orphanet_98856 |
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Systemic mastocytosis with associated hematologic neoplasm
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Orphanet_98849 |
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Myelodysplastic neoplasm with low blasts
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Orphanet_98826 |
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