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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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Hemolytic anemia due to an erythroenzymopathy
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Orphanet_98374 |
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Male infertility due to gonadal dysgenesis
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Orphanet_98313 |
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Male infertility due to impaired sperm transport
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Orphanet_98343 |
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Constitutional anemia due to iron metabolism disorder
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Orphanet_98360 |
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Male infertility due to obstructive azoospermia
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Orphanet_98343 |
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Male infertility due to testicular dysgenesis
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Orphanet_98313 |
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Rare constitutional hemolytic anemia due to an enzyme disorder
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Orphanet_98369 |
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Autosomal dominant isolated diffuse palmoplantar hyperkeratosis
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Orphanet_98349 |
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Autosomal recessive isolated diffuse palmoplantar hyperkeratosis
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Orphanet_98356 |
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Autosomal dominant isolated diffuse palmoplantar keratoderma
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Orphanet_98349 |
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Autosomal recessive isolated diffuse palmoplantar keratoderma
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Orphanet_98356 |
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Familial partial lipodystrophy
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Orphanet_98306 |
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Idiopathic interstitial pneumonia
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Orphanet_98300 |
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Embryonic testicular regression syndrome
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Orphanet_983 |
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Testicular regression syndrome
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Orphanet_983 |
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