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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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Distomatosis
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Orphanet_1685 |
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Distomiasis
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Orphanet_1685 |
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SIDDT
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Orphanet_168593 |
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sdCHC
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Orphanet_168577 |
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Fluke infection
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Orphanet_1685 |
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H syndrome
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Orphanet_168569 |
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Stomatin-deficient cryohydrocytosis
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Orphanet_168577 |
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Mudd's disease
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Orphanet_168598 |
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CHC type 2
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Orphanet_168577 |
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Spondylometaphyseal dysplasia, A4 type
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Orphanet_168555 |
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Hereditary North American Indian childhood cirrhosis
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Orphanet_168583 |
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Spondylometaphyseal dysplasia, Golden type
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Orphanet_168544 |
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Methionine adenosyltransferase I/III deficiency
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Orphanet_168598 |
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Sudden infant death-dysgenesis of the testes syndrome
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Orphanet_168593 |
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MAT I/III deficiency
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Orphanet_168598 |
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