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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.
Hereditary cystatin C amyloid angiopathy
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Orphanet_100008 |
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ABeta amyloidosis, Dutch type
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Orphanet_100006 |
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Semantic variant PPA
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Orphanet_100069 |
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Non-fluent variant PPA
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Orphanet_100070 |
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ACE inhibitor-related acquired angioedema
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Orphanet_100057 |
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NET of anal canal
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Orphanet_100082 |
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Inherited estrogen-associated angioedema
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Orphanet_100054 |
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Inherited estrogen-dependent angioedema
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Orphanet_100054 |
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ACEI-related acquired angioedema
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Orphanet_100057 |
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Renin-angiotensin-aldosterone system-blocker-induced angioedema
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Orphanet_100057 |
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F12-related hereditary angioedema with normal C1Inh
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Orphanet_100054 |
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Inherited estrogen-associated angioneurotic edema
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Orphanet_100054 |
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Inherited estrogen-dependent angioneurotic edema
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Orphanet_100054 |
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Progressive non-fluent aphasia
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Orphanet_100070 |
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NEN of appendix
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Orphanet_100079 |
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