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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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Schöpf-Schulz-Passarge syndrome
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Orphanet_50944 |
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Blomstrand chondrodysplasia
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Orphanet_50945 |
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Blomstrand osteochondrodysplasia
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Orphanet_50945 |
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PME type 2
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Orphanet_501 |
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Alkaline ceramidase 3 deficiency
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Orphanet_502444 |
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Proximal monosomy 4q25
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Orphanet_502437 |
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Serotonin-producing pancreatic NET
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Orphanet_506090 |
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Poorly-differentiated pancreatic NEN
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Orphanet_506098 |
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Functioning well-differentiated NEN of pancreas
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Orphanet_506060 |
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Non-functioning well-differentiated NEN of pancreas
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Orphanet_506075 |
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Functioning pancreatic NET
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Orphanet_506060 |
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Non-functioning pancreatic NET
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Orphanet_506075 |
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Cerebrorenal syndrome, Perez type
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Orphanet_505242 |
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Mixed neuroendocrine and non-neuroendocrine neoplasm of pancreas
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Orphanet_506112 |
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Jejunal atresia-microcephaly-ocular anomalies syndrome
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Orphanet_506307 |
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