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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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Non-syndromic non-specific multisutural craniosynostosis
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Orphanet_620158 |
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Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3
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Orphanet_62 |
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Acute flaccid myelitis
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Orphanet_623801 |
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SBDS-related severe neonatal SMD
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Orphanet_622934 |
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SBDS-related severe neonatal spondylometaphyseal dysplasia
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Orphanet_622934 |
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Familial multiple nevi flammei
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Orphanet_624 |
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Rare genetic nevus
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Orphanet_622914 |
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Congenital pigmented nevus
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Orphanet_626 |
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Non-syndromic synostosis of all cranial vault sutures
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Orphanet_620212 |
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Isolated frontal plagiocephaly
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Orphanet_620102 |
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Isolated occipital plagiocephaly
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Orphanet_620113 |
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Familial multiple port-wine stains
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Orphanet_624 |
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Paraneoplastic isolated rhombencephalitis
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Orphanet_624190 |
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Paraneoplastic isolated rhomboencephalitis
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Orphanet_624190 |
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Isolated unilateral sphenofrontal suture synostosis
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Orphanet_620139 |
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