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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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Albright hereditary osteodystrophy-like syndrome
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Orphanet_1001 |
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Neurogenic thoracic outlet compression syndrome
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Orphanet_100073 |
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Neurogenic thoracic outlet syndrome
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Orphanet_100073 |
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Hereditary spastic paraparesis type 15
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Orphanet_100996 |
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X-linked spastic paraplegia type 16
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Orphanet_100997 |
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Soft tissue perineurioma
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Orphanet_100002 |
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Scalp defects-postaxial polydactyly syndrome
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Orphanet_1003 |
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Semantic primary progressive aphasia
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Orphanet_100069 |
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Autosomal dominant pure HSP
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Orphanet_100980 |
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Autosomal recessive pure HSP
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Orphanet_100982 |
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Autosomal dominant pure SPG
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Orphanet_100980 |
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Autosomal recessive pure SPG
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Orphanet_100982 |
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Autosomal dominant pure spastic paraplegia
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Orphanet_100980 |
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Autosomal recessive pure spastic paraplegia
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Orphanet_100982 |
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Neurogenic cervical rib syndrome
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Orphanet_100073 |
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