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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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Rare thyroid carcinoma
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Orphanet_100088 |
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Lissencephaly with cerebellar hypoplasia type A
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Orphanet_100011 |
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Lissencephaly with cerebellar hypoplasia type B
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Orphanet_100012 |
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Lissencephaly with cerebellar hypoplasia type C
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Orphanet_100013 |
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Lissencephaly with cerebellar hypoplasia type D
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Orphanet_100014 |
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Lissencephaly with cerebellar hypoplasia type E
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Orphanet_100015 |
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Lissencephaly with cerebellar hypoplasia type F
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Orphanet_100016 |
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Mosaic trisomy chromosome 3
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Orphanet_100071 |
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Esophageal duplication cyst
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Orphanet_100047 |
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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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