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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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ARCL1C
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Orphanet_221145 |
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ASSA
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Orphanet_221120 |
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Hypertelorism-hypospadias-polysyndactyly syndrome
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Orphanet_2211 |
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Naguib-Richieri-Costa syndrome
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Orphanet_2211 |
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Cranial neuralgia
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Orphanet_221109 |
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Facial neuralgia
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Orphanet_221109 |
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Gerstmann syndrome
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Orphanet_221117 |
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Pseudoaminopterin syndrome
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Orphanet_221120 |
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Fowler vasculopathy
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Orphanet_221126 |
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Roifman-Chitayat syndrome
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Orphanet_221139 |
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Urban-Rifkin-Davis syndrome
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Orphanet_221145 |
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Proliferative vasculopathy and hydranencephaly/hydrocephaly
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Orphanet_221126 |
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Confetti-like macular atrophy
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Orphanet_221142 |
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Autosomal recessive cutis laxa type 1C
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Orphanet_221145 |
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Cerebral proliferative glomeruloid vasculopathy
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Orphanet_221126 |
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