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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.
DBQD
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Orphanet_1425 |
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OSMED
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Orphanet_1427 |
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Chondrodysplasia-pseudohermaphroditism syndrome
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Orphanet_1422 |
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Nivelon-Nivelon-Mabille syndrome
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Orphanet_1422 |
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Maroteaux-Stanescu-Cousin syndrome
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Orphanet_1423 |
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Desbuquois dysplasia
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Orphanet_1425 |
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Desbuquois syndrome
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Orphanet_1425 |
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Greenberg dysplasia
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Orphanet_1426 |
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HEM dysplasia
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Orphanet_1426 |
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Otospondylomegaepiphyseal dysplasia
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Orphanet_1427 |
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Skeletal dysplasia, Greenberg type
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Orphanet_1426 |
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Anaplastic thyroid carcinoma
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Orphanet_142 |
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Lethal recessive chondrodysplasia
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Orphanet_1423 |
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Benign familial chorea
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Orphanet_1429 |
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Benign hereditary chorea
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Orphanet_1429 |
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