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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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ACDMPV
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Orphanet_210122 |
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DIRA
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Orphanet_210115 |
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OMPP
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Orphanet_210115 |
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Intermediate osteopetrosis
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Orphanet_210110 |
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Urocanic aciduria
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Orphanet_210128 |
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Adult HCC
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Orphanet_210159 |
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Interleukin-1 receptor antagonist deficiency
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Orphanet_210115 |
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Congenital alveolar capillary dysplasia
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Orphanet_210122 |
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Adult hepatocellular carcinoma
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Orphanet_210159 |
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Developmental delay-hypotonia-extremities hypertrophy syndrome
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Orphanet_2101 |
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Autosomal recessive intermediate osteopetrosis
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Orphanet_210110 |
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Congenital lethal myopathy, Compton-North type
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Orphanet_210163 |
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Sterile multifocal osteomyelitis with periostitis and pustulosis
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Orphanet_210115 |
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Inherited congenital spastic quadriplegia
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Orphanet_210141 |
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Inherited congenital spastic tetraplegia
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Orphanet_210141 |
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