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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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Autosomal dominant complicated SPG
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Orphanet_100979 |
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Autosomal recessive complicated SPG
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Orphanet_100981 |
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Autosomal dominant complicated spastic paraplegia
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Orphanet_100979 |
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Autosomal recessive complicated spastic paraplegia
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Orphanet_100981 |
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Esophageal duplication cyst
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Orphanet_100047 |
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Alopecia antibody deficiency
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Orphanet_1006 |
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Spastic paraplegia-retinal degeneration syndrome
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Orphanet_100996 |
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FRAXE intellectual disability
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Orphanet_100973 |
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Mu-heavy chain disease
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Orphanet_100024 |
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Alpha-heavy chain disease
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Orphanet_100025 |
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Gamma-heavy chain disease
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Orphanet_100026 |
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RAAS-blocker-induced angioneurotic edema
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Orphanet_100057 |
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Hereditary angioneurotic edema type 1
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Orphanet_100050 |
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Acquired angioneurotic edema type 1
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Orphanet_100056 |
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Hereditary angioneurotic edema type 2
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Orphanet_100051 |
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