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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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Scott-Taor syndrome
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Orphanet_1509 |
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Crane-Heise syndrome
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Orphanet_1512 |
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Craniodiaphyseal dysplasia
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Orphanet_1513 |
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Scott-Bryant-Graham syndrome
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Orphanet_1514 |
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Cranioectodermal dysplasia
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Orphanet_1515 |
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Sensenbrenner syndrome
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Orphanet_1515 |
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Cantú syndrome
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Orphanet_1517 |
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Hypertrichotic osteochondrodysplasia
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Orphanet_1517 |
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Brachycephalofrontonasal dysplasia
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Orphanet_1519 |
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Craniofrontonasal dysplasia
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Orphanet_1520 |
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Craniofrontonasal syndrome
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Orphanet_1520 |
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Webster-Deming syndrome
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Orphanet_1521 |
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Craniometaphyseal dysplasia
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Orphanet_1522 |
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Craniomicromelic syndrome
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Orphanet_1524 |
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Currarino disease
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Orphanet_1525 |
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