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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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Slipped capital femoral epiphysis
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Orphanet_399329 |
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Slipped upper femoral epiphysis
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Orphanet_399329 |
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Melanoma of choroid
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Orphanet_39044 |
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Choroidal and ciliary body melanomas
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Orphanet_39044 |
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Miyoshi muscular dystrophy type 3
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Orphanet_399096 |
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Classic Hodgkin disease
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Orphanet_391 |
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Finnish upper limb-onset distal myopathy
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Orphanet_399086 |
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Refractory celiac disease
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Orphanet_398063 |
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SURF1-related Charcot-Marie-Tooth disease type 4
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Orphanet_391351 |
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Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
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Orphanet_397744 |
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Classic Hodgkin lymphoma
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Orphanet_391 |
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Rare genetic male infertility
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Orphanet_399980 |
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Femoral head epiphysiolysis
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Orphanet_399329 |
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Ovarian malignant epithelial tumor
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Orphanet_398934 |
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Neonatal lupus erythematosus
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Orphanet_398124 |
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