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| created at |
2024-09-23 16:23:50 UTC |
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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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46,XY ovotesticular disorder of sex development
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Orphanet_325345 |
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Sex chromosome disorder of sex development
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Orphanet_325546 |
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Genetic 46,XX disorder of sex development
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Orphanet_325697 |
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Genetic 46,XY disorder of sex development
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Orphanet_325706 |
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Genetic 46,XY disorder of sex development of endocrine origin
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Orphanet_325713 |
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46,XY DSD due to LHB deficiency
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Orphanet_325448 |
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46,XY DSD due to a cholesterol synthesis defect
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Orphanet_325511 |
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46,XY DSD due to impaired androgen production
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Orphanet_325357 |
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46,XY DSD due to luteinizing hormone subunit beta deficiency
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Orphanet_325448 |
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Cleft lip/palate-ectodermal dysplasia syndrome
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Orphanet_3253 |
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DSD of gynecological interest
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Orphanet_325620 |
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Leydig cell hypoplasia due to LHB deficiency
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Orphanet_325448 |
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46,XX DSD induced by endogenous maternal-derived androgen
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Orphanet_325093 |
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46,XX DSD induced by exogenous maternal-derived androgen
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Orphanet_325099 |
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46,XX DSD induced by fetoplacental androgens excess
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Orphanet_325061 |
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