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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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Del(2)(q37)
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Orphanet_1001 |
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Deletion 2q37
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Orphanet_1001 |
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Monosomy 2q37qter
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Orphanet_1001 |
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Thymic tumor
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Orphanet_100100 |
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Albright hereditary osteodystrophy type 3
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Orphanet_1001 |
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Albright hereditary osteodystrophy-like syndrome
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Orphanet_1001 |
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2q37 microdeletion syndrome
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Orphanet_1001 |
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Brachydactyly-intellectual disability syndrome
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Orphanet_1001 |
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Neuroendocrine tumor with other location
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Orphanet_100101 |
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