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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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Furunculoid myiasis due to Cordylobia rodhaini
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Orphanet_563690 |
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Furunculous myiasis due to Cordylobia rodhaini
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Orphanet_563690 |
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Furuncular myiasis due to Dermatobia hominis
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Orphanet_563684 |
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Furunculoid myiasis due to Dermatobia hominis
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Orphanet_563684 |
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Furunculous myiasis due to Dermatobia hominis
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Orphanet_563684 |
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Multiple mitochondrial dysfunctions syndrome type 5
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Orphanet_569274 |
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Multiple mitochondrial dysfunctions syndrome type 6
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Orphanet_569290 |
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Generalized lymphatic dysplasia of Fotiou
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Orphanet_568062 |
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Neonatal osseous dysplasia type 1
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Orphanet_56304 |
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POMGNT2-related muscular dystrophy
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Orphanet_565899 |
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Limb-girdle muscular dystrophy type D4
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Orphanet_565909 |
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Limb-girdle muscular dystrophy type R24
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Orphanet_565899 |
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FOXG1-related epileptic-dyskinetic encephalopathy
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Orphanet_561854 |
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Transmissible spongiform encephalopathy
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Orphanet_56970 |
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Autosomal recessive extra-oral halitosis
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Orphanet_562538 |
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