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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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CVIC
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Orphanet_641829 |
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MMNCB
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Orphanet_641 |
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VEOS
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Orphanet_641496 |
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Imprinting disorders
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Orphanet_641343 |
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PAPASH syndrome
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Orphanet_641380 |
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PASS syndrome
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Orphanet_641385 |
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PsAPASH syndrome
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Orphanet_641390 |
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CNS tuberculosis
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Orphanet_641396 |
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Childhood-onset schizophrenia
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Orphanet_641496 |
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Endogenous CS
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Orphanet_641613 |
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Autosomal recessive HIES due to ZNF341 deficiency
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Orphanet_641368 |
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Syndrome de Volkmann congénital
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Orphanet_641829 |
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HPDL-related Leigh-like encephalopathy
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Orphanet_641353 |
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Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency
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Orphanet_641368 |
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Immunotherapy induced hypophysitis
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Orphanet_641350 |
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