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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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Ig-mediated MPGN
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Orphanet_329903 |
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Immunoglobulin-mediated MPGN
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Orphanet_329903 |
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C3 glomerulopathy
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Orphanet_329918 |
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Non-Ig-mediated MPGN
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Orphanet_329918 |
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Non-immunoglobulin-mediated MPGN
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Orphanet_329918 |
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C3 glomerulonephritis
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Orphanet_329931 |
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Intermittent hydrarthrosis
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Orphanet_329967 |
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TNF receptor 1-associated periodic syndrome
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Orphanet_32960 |
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Syndrome with 46,XX DSD
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Orphanet_325109 |
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Syndrome with 46,XX difference of sex development
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Orphanet_325109 |
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Syndrome with 46,XX disorder of sex development
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Orphanet_325109 |
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Syndactyly type 7
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Orphanet_3258 |
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ABeta amyloidosis, Arctic type
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Orphanet_324723 |
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Autosomal dominant Charcot-Marie-Tooth disease type 2Q
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Orphanet_329258 |
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46,XY ovotesticular DSD
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Orphanet_325345 |
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