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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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JBTS with JATD
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Orphanet_397715 |
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Transient neonatal acquired myasthenia
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Orphanet_391504 |
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Appendiceal mucinous adenocarcinoma
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Orphanet_391723 |
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Ovarian mucinous adenocarcinoma
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Orphanet_398961 |
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Clear cell adenocarcinoma of the ovary
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Orphanet_398971 |
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PrP systemic amyloidosis
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Orphanet_397606 |
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Hereditary sensory and autonomic neuropathy type 7
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Orphanet_391397 |
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Hereditary sensory and autonomic neuropathy type VII
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Orphanet_391397 |
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Neonatal antiphospholipid antibody syndrome
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Orphanet_398097 |
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Hereditary isolated aplastic anemia
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Orphanet_397692 |
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Giant cell arteritis
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Orphanet_397 |
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Disorder of asparagine metabolism
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Orphanet_391381 |
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Autosomal spastic ataxia type 2
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Orphanet_397946 |
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Short stature-optic atrophy-Pelger-Huët anomaly syndrome
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Orphanet_391677 |
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Secondary neonatal autoimmune disease
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Orphanet_398091 |
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