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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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Rare genetic skin disease
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Orphanet_68346 |
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Autosomal dominant spastic paraplegia type 80
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Orphanet_631068 |
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Autosomal recessive spastic paraplegia type 82
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Orphanet_631073 |
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Autosomal recessive spastic paraplegia type 83
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Orphanet_631076 |
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Autosomal recessive spastic paraplegia type 84
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Orphanet_631079 |
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Autosomal recessive spastic paraplegia type 85
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Orphanet_631082 |
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Autosomal recessive spastic paraplegia type 86
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Orphanet_631085 |
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Autosomal recessive spastic paraplegia type 87
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Orphanet_631088 |
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Placenta accreta spectrum
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Orphanet_662721 |
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Placenta accreta spectrum disorder
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Orphanet_662721 |
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Isolated unilateral sphenofrontal suture synostosis
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Orphanet_620139 |
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Chaotic conus spinal cord lipoma
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Orphanet_645285 |
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Extramedullary conus spinal cord lipoma
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Orphanet_645297 |
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Intramedullary non-dysraphic spinal cord lipoma
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Orphanet_645359 |
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Conus sparing spinal cord lipoma
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Orphanet_645362 |
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