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| created at |
2024-09-23 16:23:50 UTC |
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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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FNAIT
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Orphanet_853 |
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MRXS9
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Orphanet_85324 |
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NAIT
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Orphanet_853 |
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Johnson syndrome
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Orphanet_85320 |
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Martin-Probst syndrome
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Orphanet_85321 |
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Aldred syndrome
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Orphanet_85332 |
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Fried syndrome
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Orphanet_85335 |
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X-linked deafness-intellectual disability syndrome
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Orphanet_85321 |
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X-linked intellectual disability, Pai type
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Orphanet_85322 |
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X-linked intellectual disability, Seemanova type
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Orphanet_85323 |
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X-linked intellectual disability, Shrimpton type
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Orphanet_85324 |
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X-linked intellectual disability, Stevenson type
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Orphanet_85325 |
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X-linked intellectual disability, Stoll type
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Orphanet_85326 |
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X-linked intellectual disability-ataxia-apraxia syndrome
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Orphanet_85338 |
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X-linked intellectual disability-retinitis pigmentosa syndrome
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Orphanet_85332 |
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