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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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Dermoodontodysplasia
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Orphanet_1660 |
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PCH4
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Orphanet_166063 |
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PCH6
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Orphanet_166073 |
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Olivopontocerebellar hypoplasia
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Orphanet_166063 |
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Metaphyseal chondrodysplasia, Kaitila type
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Orphanet_166038 |
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Von Willebrand disease type 1
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Orphanet_166078 |
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Von Willebrand disease type 2
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Orphanet_166081 |
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Von Willebrand disease type 2A
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Orphanet_166084 |
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Von Willebrand disease type 2B
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Orphanet_166087 |
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Von Willebrand disease type 2M
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Orphanet_166090 |
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Von Willebrand disease type 2N
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Orphanet_166093 |
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Von Willebrand disease type 3
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Orphanet_166096 |
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Multiple epiphyseal dysplasia due to collagen 9 anomaly
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Orphanet_166002 |
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Multiple epiphyseal dysplasia with Robin phenotype
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Orphanet_166016 |
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Multiple epiphyseal dysplasia, Al-Gazali type
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Orphanet_166024 |
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