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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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Autosomal dominant Charcot-Marie-Tooth disease type 2L
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Orphanet_99945 |
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Ovarian malignant Sertoli-Leydig cell tumor
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Orphanet_99916 |
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House allergic alveolitis
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Orphanet_99907 |
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Occupational allergic alveolitis
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Orphanet_99909 |
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Hereditary motor and sensory neuropathy, Lom type
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Orphanet_99950 |
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Hereditary motor and sensory neuropathy, Russe Type
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Orphanet_99953 |
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Granulosa cell cancer
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Orphanet_99915 |
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Esophageal epidermoid carcinoma
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Orphanet_99977 |
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Squamous cell carcinoma of the esophagus
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Orphanet_99977 |
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Ovarian Sertoli-Leydig cell cancer
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Orphanet_99916 |
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Dysgerminomatous germ cell cancer of the ovary
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Orphanet_99912 |
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Theca (steroid-producing) cell cancer, not further specified
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Orphanet_99917 |
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Esophageal squamous cell carcinoma
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Orphanet_99977 |
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Malignant granulosa cell tumor of the ovary
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Orphanet_99915 |
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Malignant Sertoli-Leydig cell tumor of the ovary
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Orphanet_99916 |
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